US3306291A - Disposable sterile syringes, needle containers and the like having prestressed frangible portions therein - Google Patents

Description

3,306,291 AND F 8, 1967 e. K. BURKE DISPOSABLE STERILE SYRINGES, NEEDLE CONTAINERS I THE LIKE HAVING PRESTRESSED FRANGIBLE PORTIONS THEREIN 6 Sheets-Sheet 1 Filed April 14, 1964 INVENTOR GEORGE K. BURKE ATTORNEYS RKE 3,306,291 NEEDLE CONTAINERS AND TRES SED FRANGI BLE Feb. 28, 1967 BU DISPOSABLE STERILE SYRLNGES THE LIKE HAVING PRES PORTIONS THEREIN 6 Sheets-Sheet 2 Filed April 14, 1964 E mu U m8 MK E G R O E G Q: E i 02 k W cm I I O3 /J l l bnmw I 2 p NE ATTORNEYS G. K. BURKE Feb. 28, 1967 DISPOSABLE STERILE SYRINGES, NEEDLE CONTAINERS AND THE LIKE HAVING PRESTRESSED FRANGIBLE PORTIONS THEREIN Filed April 14, 1964 6 Sheets-Sheet 3 I NV ENT OR ATTORNEYS GEDRGEKBURKE Feb. 28, 1967 K. BURKE G v DISPOSABLE STERILE SYRINGES, NEEDLE CONTAINERS AND THE LIKE HAVING PRESTRESSED FRANGIBLE PORTIONS THEREIN Filed April 14, 1964 6 Sheets-Sheet 5 INVENTOR GEORGE KBURKE BY% MW ATTORNEYS G K. BURKE DISPOSABLE STERILE S X'RINGES, NEEDLE CONTAINERS AND THE LIKE HAVING PRESTRESSED FRANGIBLE PORTIONS THEREIN 6 Sheets-Sheet 6 IIIJ INVENTOR GEORGE K. BURKE ATTORNEYS United States Patent 3,306,291 DISPOSABLE STERHLE SYRINGES, NEEDLE CONTAlNEl-XS AND THE LIKE HAVING PRESTRESSED FRANGHBLE PORTIONS THEREIN George K. Burke, Bethlehem, Pa., assignorto Barron Medical Products, Inc., Bethlehem, Pa, a corporation of Pennsylvania Filed Apr. 14, 1964, Ser. No. 359,674 41 Claims. ((31. 128218) The present invention relates to a new and novel disposable sterile device, and more particularly to a sterile device which is adapted to be effectively destroyed after a single use thereof so as to prevent re-use of the apparatus for the intended function.

The present invention is directed particularly to the medical field wherein it is of primary consideration to provide apparatus which is sterile and which remains sterile up until the time of use. In the present invention the particular disposable device may comprise either a throw away syringe or a hypodermic needle container or package. In either event, these devices are adapted to be used once for the intended use and then broken away in such a manner as to prevent effective re-use thereof for the same purpose.

It is a particular important feature of the present invention that the disposable device includes a frangible portion which enables part of the device to be broken away in such a manner that it cannot 'be placed back in its original position and serve its original purpose. In the case of a disposable syringe, the boss portion upon which the hypodermic needle is positioned is broken off, and in the case of the needle container, the cap of the container is broken off. I

Disposable devices of a similar nature have been provided in the prior art, and the materials employed in such devices have been generally of a nature such that they can be readily broken. For example, disposable syringes have been manufactured of polystyrene plastic and provided with a weakened area by forming an indentation therein which permits this type of material to be readily broken.

However, the materials employed for similar devices in the prior art have not proved satisfactory due to other characteristics thereof. Such prior art materials have not proven to always be inert to the solvents and carriers as may be used in medicaments, and accordingly, in many instances the specifications for this type of apparatus requires the use of a different type of material. The present invention employs a more desirable type of material insofar as being inert to solvents and carriers is concerned. For example, a particular substance which may be used is polypropylene plastic. This material meets all of the present-day specifications and requirements for this type of apparatus, but it presents a particular problem in that it does not readily break and is not of a brittle nature, but rather is somewhat flexible and very difiicult to break off. This is true even though the wall thicknesses may be weakened or made quite thin under normal molding techniques. This has proved to be the case in actual use since supposedly disposable devices of this nature have been manufactured of polypropylene or similar substances and have exhibited the characteristic that they are extremely difficult to break away or destroy in the field, and accordingly they have not proved satisfactory due to this characteristic.

The present invention employs a unique concept in providing a frangible or break-away portion in polypropylene material or material of a similar nature. In the present invention, the frangible portion is afforded 3,305,291 Patented Feb. 28, 1967 by molding the area which it is desired to break away in a very particular and special manner. t

It is a specific object of the present invention to pro-. vide a frangible area in polypropylene or similar material by creating areas of stress which are prone to structural weakness when subjected to external forces as by manually bending this particular portion. In order to obtain the desired internal stresses and concentration of stresses in the frangible area, the wall portion at this particular area is appreciably less in thickness than the thickness of the adjacent wall portions of the apparatus.- i

In addition, the length of the stress area should be approximately the same as the thickness of the wall at the frangible portion and under no circumstances should the length of the stress area be more than twice the thickness of the wall. i

In order to provide the desired pre-stressed area, the mold is so designed that the finished product which com prises a body means having a frangible area includes an annular shoulder formed on the inner and outer surfaces of the body means. Each of these annular shoulders is, defined by a surface which extends substantially 90 degrees to the associated inner or outer surface. These shoulders are also offset longitudinally of the body means. This particular portion of the body means is additionally designed so that the surfaces of the shoulders should define an angle of approximately degrees with respect to a line drawn between the closest points of the internal corners defined by the shoulders as will be hereinafter more fully explained.

The disposable syringe of the present invention is utilized only one time and then broken away so as not to. be reused. The syringe is initially sterilized as by chemical gas or the like, and the syringe may comprise a sterile package until used for administering a dosage .of suitable medicament. It is of course apparent that the construction of the syringe must be extremely inexpensive in order to provide a practical economic situation, and accordingly the present invention is especially constructed of relatively inexpensive materials which can be quickly and easily;

assembled.

The utilization of the disposable syringe according to the present invention saves considerable time which is normally involved in processing sterilizing equipment when using syringes whichare not disposable, and in addi tion, the syringe ofthe present invention is quite convenient to use and providesmaximum comfort for the patient particularly in view of the fact that a new sharp.

needle is used for every injection.

In many applications, it is quite important to obtain a very accurate reading as to enable exact dosages to be given. In order to accomplish this result, the barrel tation with the plunger so that very fine adjustment of the piston means and plunger may be obtained by twisting the piston means within the barrel.

can only be made by a lateral movement of the plunger which generally cannot be accomplished in very smooth degrees as is possible when the piston can be twisted and moved longitudinally at the same time.

The piston means is additionally provided with 'external ribs or rings thereon which engage the inner surface of the barrel and one of the rings having a very sharp corner or edge or line thereon which enables an accurate visible indication to be obtained of the exact. I

position of the piston means within the barrel.

It will be 'recognized that if the plunger is rotatable with respect to the I piston means, the fine adjustment of the piston means It is also important to provide a syringe arrangement which assures that substantially all of the medicament is expelled therefrom when the plunger is pushed inwardly.

In order to accomplish this result, the inner end wall of the barrel is of a generally concave configuration and the resilient piston means is of a similar complementary configuration so as to fit relatively snugly with the inner end wall at the innermost limit of movement of the plunger. This arrangement assures that all of the medicament will be expelled from the barrel. In one modification of the present invention, the syringe is provided with an auxiliary means in the form of a skirt extending from the barrel for ensuring that the hypodermic needle remains in place on the boss of the syringe, The needle is normally retained in place by means of a conventional tapered arrangement, and the skirt additionally assures that the needle will remain in its proper position. The skirt further provides a shoulder for attachment of the needle guard, thus reducing the area of medicament loss by about -inch or more.

A further modified form of the syringe provides an arrangement wherein a space is provided within the piston means and the associated end portion of the plunger such that the hydraulic forces developed during use of the device can flatten out the piston means and assure that it is pressed very tightly against the inner wall of the barrel.

The needle container of the present invention as discussed previously provides asterile atmosphere for retaining the supported hypodermic needle in a sterile condition, and in addition, the needle container is specifically designed so as to be positively tamper-proof. In order to accomplish this, the needle container includes a pair of portions which snap into engagement with one another and effectively lock together so that they cannot be taken apart without completely destroying the parts. One of the portions of which the needle container is constructed is provided with the aforesaid frangible portion so as to permit this particular part of the container to be broken away and permanently destroyed so that it cannot be re-used.

An object oi the present invention is to provide a new andnovel disposable sterile device which provides a sterile package and which remains in a sterile condition until used, and further which is especially adapted to be used just one time and then thrown away and discarded.

Another object of the invention is to provide a disposable sterile device including means for effectively destroying the device to prevent re-use thereof for the inr tended purpose.

A further object of the invention is the provision of a disposable syringe which saves the time of a user, which is quite convenient to use and which provides a maximum degree of comfort for the patient while eliminating the danger of cross contamination.

Yet another object of the invention is to provide a disposable syringe including means for providing a very sharp line to give an accurate reading of exact dosages and further which is so constructed as to permit very fine adjustment of the position of the piston means within the barrel.

A still further object of the invention is the provision of a disposable syringe including means for effectively filtering the aspirated air and for assuring that all of the medicament is expelled during use.

Still another object of the invention is the provision of a disposable syringe in one modification which includes auxiliary means to hold the needle in place and to attach the needle guard, and in another modification which includes an arrangement to enable hydraulic pressure to urge the piston means tightly against the sides of the barrel.

Still another object of the invention is to provide a disposable needle container which is sterile and which is substantially tamper-proof and must be destroyed in order to open.

Other objects and many attendant advantages of the invention will become more apparent when considered in connection with the specification and accompanying drawings, wherein:

FIG. 1 is a perspective view of a first modification of a disposable syringe according to the present invention;

FIG. 2 is a longitudinal section taken through the syringe shown in FIG. 1;

FIG. 3 is a sectional exploded view illustrating the details of construction of the syringe;

FIG. 4 is a sectional view taken substantially along line 4-4 of FIG. 2 looking in the direction of the arrows;

FIG. 5 is a view taken along line 5-5 of FIG. 3 looking in the direction of the arrows;

FIG. 6 is a view partly in section taken substantially along line 6-6 of FIG. 3 looking in the direction of the arrows;

FIG. 7 is a longitudinal section partly broken away through a second modification of the present invention;

FIG. 8 is an enlarged exploded view principally in section illustrating the details of construction of various of the components shown in FIG. 7.

FIG. 9 is a view taken substantially along line 9-9 of FIG. 8 looking in the direction of the arrows;

FIG. 10 is a view partly in section taken substantially along line 10-10 of FIG. 8 looking in the direction of the arrows; 1

FIG. 11 is a view taken substantially along line 11-11 of FIG. 7 looking in the direction of the arrows;

FIG. 12 is a longitudinal sectional view partly broken away illustrating a third modified form of the disposable syringe;

FIG. 13 is an enlarged exploded view principally in section illustrating the details of construction of certain components of the structure shown in FIG. 12;

FIG. 14 is a View taken substantially along line 14-14 of FIG. 13 looking in the direction of the arrows;

FIG. 15 is a view taken substantially along line 15-15 of FIG. 13 looking in the direction of the arrows;

FIG. 16 is a view taken substantially along line 16-16 of FIG. 13 looking in the direction of the arrows;

FIG. 17 illustrates an adapter means positioned over the end of the barrel shown in FIG. 12;

FIG. 18 is a longitudinal section through a fourth modified form of the disposable syringe according to the present invention;

FIG. 19 is a sectional view taken substantially along line 19-19 of FIG. 18 looking in the direction of the arrows;

FIG. 20 is an enlarged exploded view principally in section illustrating the details of construction of certain of the components shown in FIG. 18;

FIG. 21 is a sectional view taken substantially along line 21-21 of FIG. 20 looking in the direction of the arrows;

FIG. 22 is a sectional view taken substantially along line 22-22 of FIG. 20 looking in the direction of the arrows;

FIG. 23 is a view partly broken away illustrating the indicia on the barrel and the manner in which the piston means provides a very clear and accurate reading as to its relative position;

FIG. 24 is a top perspective view of a needle container according to the present invention;

FIG. 25 is a view similar to FIG. 24 illustrating the manner in which the end portion of the body means is adapted to be broken away to expose the hub of the needle;

FIG. 26 is a sectional view taken substantially along line 26-26 of FIG. 24 looking in the direction of the arrows;

FIG. 27 is a sectional view taken substantially along line 2727 of FIG. 26 looking in the direction of the arrows;

FIG. 28 is a sectional view taken substantially along line 2828 of FIG. 26 looking in the direction of the arrows;

FIG. 29 is an enlarged view illustrating the details of construction of the frangible portion of the body means;

FIG. 30 illustrates a longitudinal sectional view of the modified form of the body means of the needle container of the present invention;

. FIG. 31 is a longitudinal sectional view of a modified form of the enclosure means of the needle container, and;

FIG. 32' is 'a longitudinal section through a modified form of the invention employing a unique arrangement for retaining the needle hub in position on the body means of a syringe.

Referring now to the drawings wherein like reference characters designate corresponding parts throughout the several views,'there is shown in FIGS. 1 through 6 inclusive a first modification of the invention which may I for example comprise atuberculin type 1 cc. syringe. This syringe includes a barrel or body means 40 which is formed of a material which is normally difiicult to break such as polypropylene having the desired characteristics mentioned hereinbefore. This barrel is transparent or nearly. so and is provided with suitable indicia thereon as indicated generally by reference numeral 41. The barrel is provided with an integral laterally extending flange portion, 42 at one end thereof terminating in abead 44, this flange portion serving as an area for gripping by the fingers of an operator and also preventing rolling by having opposite fiat sides.

Aboss 46 projects longitudinally from the opposite end of the barrel and is indicated byreference numeral 46, it being noted that the boss is of less cross sectional dimension than the barrel, the boss being interconnected with the barrel by a frangible portion indicated generally by reference numeral 47 and which will be described more fully hereinafter.

The boss is provided with ataper 48 on the outer surface thereof which may comprise a Luer taper of well known construction for receiving the hub portion of a hypodermic needle having a cooperating taper and for retaining the hypodermic needle thereon. Theinner end Wall 50 of the ball is of a generally arcuate configuration and may for example comprise a portion of a spherical.

surface, this inner end wall having arecess 52 formed adjacent thereto and in communication with abore 54 extending longitudinally through the boss.

Referring now particularly to FIG. 3 of the drawings,

the details of construction of the frangible portion 47 may be more clearly understood. As mentioned previ-.

ously, the barrel is formed of a material such as polypropylene which is normally very difiicult to break. In order to render this frangible portion readily breakable by manual effort, this frangible portion is so constructed as to have built-in internal stresses wherein the stresses are concentrated in the frangible portion area, this prestressed area providing a portion which is prone to structural weakness when subjected to external forces such as bending.

The frangible portionis formed by providing the annular shoulders and 62 on the outer and inner surfaces of the barrel means respectively. It will of course be realized that the surface ofshoulder 62 is formed within the boss portion of the barrel and that shoulder 60 is formed at the end of the barrel as seen in FIG. 3. The particular locations of these shoulders may be varied as will become apparent in connection with the description of the other modifications of the invention, but in each case certain critical relationships exist.

Each of the annular shoulders defines an angle of approximately 90 degrees with respect to the associated inner surface of the barreL' In other words, the angles a and b as seen in FIG. 3 are substantially 90 degrees.

5 The corners as defined adjacent the frangible areas are sharp, and two internal corners as indicated byreference numerals 64 and 66 are defined by theshoulders 60 and 62 respectively where these shoulders intersect the associated surfaces.

It will be realized that a particular object of this construction is to cause the stresses to be concentrated in the thin wall area defined between the inner and outer surfaces of the barrel and between the planes defined by theannular shoulders 66 and 62. It should be noted that the thickness of the wall portion of the frangible area as defined between these limits as set forth above its appreciably less than the thickness of the adjacent wall portions on either side of the thin wall area. It has been found that the length of this stress area extending longitudinally of the barrel should be approximately the same dimension as the thickness of the thin wall pre-stressed frangible area, and under no circumstances should the length of the stress area be more than twice the thickness of this thin wall area.

A phantom line x-x has been drawn between the twointernal corners 64 and 66. This line has been drawn between the closest points on these two internal corners, and it will be noted that the various surfacesas do the outer and inner surfaces of the barrel adjacent 30 thereto.

The principal reason for the development of the desired internal stresses in this frangible area in this type of material is the sudden change in wall thickness which causes uneven and different cooling rates during the molding operation, and subsequent further cooling after the molded part has been removed from the mold. Sometimes it may require a few minutes to several hours for final cooling and formation of maximum internal stresses. Since shrinkage accompanies this cooling, the internal stresses are developed. There are no appreciable radii formed adjacent the frangible area, but rather the corners are.

sharp. The material employed is of high melt index and of low molecular weight and is hard flowing and sets up very quickly in the mold. The mold area around thefrangible portion is maintained quite cold during the molding operation and high pressure is utilized to pack the plastic material into the mold when filling the cavities. These techniques cause the desired formation of stresses when the structure is designed as illustrated hereconstruction as discussed above which develops the de-.

sired internal stresses at the frangible portion, this frangible portion can be'readily broken with just an average.

amount of manual effort. Accordingly the present invention provides a unique manner of affording the desired characteristic of forming a readily breakable area,

at a particular portion of the structure.

A plunger is slidably disposed within the barrel and includes a main elongated substantially cylindrical portion 70 having anenlarged end portion 72 at one end thereof which is adapted to be manually engaged by the thumb or the like for operating the plunger in the usual manner. The plunger is preferably formed of a material such as high impact styrene or a similar material. A plurality of laterally extending and angularly spaced ribs 74 are provided at the enlarged end of the plunger for reinforcing and rigidifying this manually engageable end portion.

The opposite end of the plunger includes a reduced end portion indicated generally byreference numeral 76 which has a particular construction as seen most clearly in FIGS. 3 and 5. As seen in these figures, the reduced end portion includes arectangular shank portion 78 extending integrally from the main body portion of the plunger, this shank portion joining with a substantially disc-shapedportion 80. Extending outwardly fromdiscshaped portion 80 is a pair of spacedportions 82 and 84 defining agroove 86 therebetween. The outer surfaces ofportions 82 and 84 includefiat surfaces 90 and 92 each of which is substantially frusto-triangular in configuration as seen in FIG. 3 and which additionally is sloped as seen in FIG. 5 so as to define an oblique angle with respect to the longitudinal axis of the plunger.

Referring now particularly to FIG. 3, a resilient piston means is provided, this piston being formed preferably of pharmaceutical or medical grade rubber or a similar substance. The piston means is provided with a recess for receiving the reduced end portion of the plunger and is completely complementary thereto. Referring now particularly to FIGS. 3 and 6, a tapered entrance portion 102 is provided into the recess of the piston means to facilitate entry of the reduced end portion, this tapered entrance portion being in communication with a longitudinally extendingrectangular bore 104 which snugly receives theportion 78 of the reduced end of the plunger. A recess portion 106 is adapted to receive the portion '80 of the reduced end of the plunger, and a rib 108 is provided in the center of the recess within the piston means, this rib 108 fitting snugly within the slot or groove 86 defined between theportions 82 and 84 of the plunger end. A pair of recesses 1G9 and 110 are provided within the piston means at either side of the rib 108 and are adapted to receive the twoportions 82 and 84 of the reduced end of the plunger. With this over-all arrangement, it is apparent that the piston means is snugly received on the end of the plunger and is movable longitudinal therewith and cannot rotate with respect to the plunger thereby enabling very fine adjustments of the apparatus.

As seen particularly in FIG. 3, theouter end 111 of the piston means is provided with a substantially arcuate configuration and may comprise a portion of a spherical surface, this configuration being substantially complementary to theinner end wall 50 of the barrel such that the piston means is adapted to fit snugly against the end of the barrel when moved to its innermost position thereby assuring that all of the medicament within the barrel will be expelled as the plunger is moved to its full in position.

A pair of peripherally extendingribs 112 and 114 are formed on the outer surface of the piston means and are adapted to engage the inner 'wall of the barrel to provide an effective fluid-tight and sterile seal therewith. Therib portion 114 is provided with a very sharp corner 116 which in operation provides a means for obtaining a very accurate and definite visual indication or definition of the exact position of the piston means with respect to the indicia formed on the barrel.

As seen particularly in FIGS. 1, 2 and 3, a needle guard is indicated generally byreference numeral 120 and may be formed for example of polyethylene or the like. A plurality of spacedribs 122 are provided on the outer surface of the needle guard to help prevent the needle guard from rolling along a supporting surface and to facilitate gripping and removal at the time of use.

The needle guard includes a main elongatedhollow body portion 124 which terminates in an enlargedopen end portion 126 fitting about thebarrel 40. A peripherally extending sealingrib 128 extends inwardly from the inner surface of the open end portion of the needle guard and engages the outer surface of the barrel for providing a frictional contact therewith which not only serves to retain the needle guard in operative position on the barrel but which also provides a sterile seal therewith. Anannular shoulder 130 formed on the inner surface of the needle guard is adapted to abut up against the end portion of the barrel as seen in FIG. 2.

The opposite end portion of the needle guard is provided with ahole 132 through which air may be aspirated into the interior of the needle guard, a rib orring portion 134 being provided at this end of the needle guard for retaining a body ofcotton 136 or other suitable filter media in positionadjacent hole 132. It is apparent that any sort of sterile filter means may be employed, and absorbent cotton is preferred for this purpose, this cotton serving to maintain any air aspirated into the needle guard in the sterile condition. Air is filtered when aspirated into the barrel before the guard is removed and the needle inserted into a multi-dose vial. Filtered air pressurizes the vial and facilitates the withdrawal of medicament. Without this air, vacuum resulting after withdrawal of medicament would tend to suck in atmospheric air with bacteria. The bacteria could eventually reduce the potency of the injectable and subsequently be injected into patients.

A conventional hypodermic needle is disposed within the needle guard and is mounted upon theboss 46 of the barrel, the needle including ahub portion 140 formed of an anodized aluminum alloy for example, this hub being knurled and having an internal taper thereon complementary to the taper formed on the outer surface ofboss 46 for retaining the hypodermic needle in operative position on the boss.

The needle also includes a hollowelongated portion 142 which terminates in asharp point 144,portion 142 being preferably formed of stainless steel or similar substance.

It is apparent that the needle guard may be mounted in operative position simply by slipping it over the barrel after the hypodermic needle has been mounted in operative position, a beveledinner edge 127 as seen in FIG. 3 being provided on the needle guard for facilitating its mounting in operative position. The apparatus is normally sterilized by utilizing a sterilizing gas such as a combination of carbon dioxide and ethylene oxide which may be used either in the proportions of 90 percent carbon dioxide, 10 percent ethylene oxide, or 80 percent carbon dioxide, 20 percent ethylene oxide. This sterilizing gas will fill the assembly during the sterilizing operation, and after having been sterilized, the sealingportion 128 will maintain a sterile seal within the needle guard in combination with the cotton filter means 136, and the piston means will also serve to provide a sterile seal with respect to the barrel thereby preventing any contamination of the hypodermic needle until the needle guard is removed for actual use of the apparatus.

It should be noted at this time that the various modifications as described hereinafter are in many respects similar to the structure discussed above, and in each case the principles involved in designing the frangible area are the same, and accordingly it is not considered necessary to repeat in detail the particular principles involved in forming the frangible area, it being realized that the same concepts are involved throughout the instant application in each of the different modifications.

Referring now particularly to FIGS. 7 through 11 inclusive, a modified form of the invention is illustrated which may comprise for example a 1 cc. insulin syringe. This particular syringe includes a barrel having amain body portion 140 formed of polypropylene or similar material and which is generally cylindrical and hollow as the previous barrel construction and transparent with indicia formed thereon. Aradially extending flange 142 is provided at the open end of the barrel adjacent abeveled portiton 143 for facilitating entry of the plunger into the barrel, abead 144 being formed at the outer surface offlange 142.

Aboss 146 projects longitudinally from the opposite end of the barrel and is provided with an outertapered surface 148 similar to the tapered surface provided on the previously described boss.Boss 146 is connected with themain body portion 140 of the barrel by afrangible portion 150.

The frangible portion 150' is constructed similar to that previously described, this frangible portion including internal stresses built thereinto and being formed by providing an outerannular shoulder 152 on the outer surface of the barrel and an innerannular shoulder 154. As in the previous modification, these shoulders define angles of substantially 90 degrees with respect to the associated outer and internal surfaces, these 90 degree angles being indicated by the angles a and b. As in the previously described modification, a line LL is drawn through the nearest points on the internal corners as indicated byreference numerals 156 and 158.

Here again, it will be noted that the thickness of the wall at the frangible portion is appreciably less than the thickness of the adjacent wall portions at either side thereof and the length of the stress area should be approximately the same dimension as the thickness of the wall and not more than twice such dimension. The surfaces defining theannular shoulders 152 and -4 as Well as the intersecting surfaces of the inner and outer surfaces of the barrel define angles of approximately 45 degrees with respect to the line L-L.

Referring particularly to FIGS. 7 and 8, a skirt portion indicated byreference numeral 160 projects longitudinally frombarrel 140 and is formed integral therewith, the outer surface of the skirt being of less cross sectional dimension than the outer surface of the barrel. An innerbeveled edge 162 is provided on the skirt, and aninner surface 164 of the skirt is spaced outwardly of the tapered outer surface of theboss 146 and provides an annular space within which is received thehub 170 of a conventional hypodermic needle. It will be noted that theenlarged end portion 171 of the hub is adapted to be clamped between the outer surface ofboss 14 6 and the inner surface of the skirt so as to securely retain the hypodermic needle in the operative position as shown. The skirt also serves to accept the needle guard. As in the previous modification, the needle may include a knurled hub portion of anodized aluminum and an elongated tubular portion 172 of stainless steel or the like which terminates in asharp point 174.

As seen particularly in FIG. 8, theinner end wall 180 of the "barrel is of generally concave arcuate configuration as in the previously described modification and may for example define a portion of the surface of a sphere. This inner end wall is in communication with arecess portion 182 which in turn is in communication with a taperedportion 184 which joins with thebore 186 formed through theboss 146. The intercooperation of the concave inner end wall and thetapered surface 184 is such as to assure that substantially all of the medicament will be expelled from the barrel.

A plunger is slidably disposed within the barrel and includes a substantially cylindricalhollow portion 190 having a radially extending flange H2 formed at one end thereof and adapted to be manually engaged as by the thumb for pushing the plunger in or for grasping by the fingers to pull the plunger out, reinforcingribs 194 being formed immediately beneathflange 192 on the outer surface of the plunger. The plunger also includes areduced end portion 196 at the opposite end thereof of novel configuration.

As seen particularly in FIGS. 8 and 9, thereduced end portion 1% of the plunger includes ashank portion 230 extending longitudinally of theplunger 1% and being integral with a disc-shapedportion 202. Extending longitudinally fromportion 202 are four spacedribs 204, 206, 298 and 210, these ribs being angularly spaced approximately 90 degrees from one another.

Each of these ribs is provided with a pair of angularly disposed outer edges, these edges being identified by the reference numerals 204', 2%, 206, 206", 2%, 268", 216, 2113" respectively. The first series ofedges 294, 206, 208' and 210 define an angle of approximately 70 degrees with respect to a plane extending perpendicular to the longitudinal axis of the plunger, or in other words these edges if extended would define an angle of approximately 20 degrees with the longitudinal axis of the plunger. Theother edges 204', 206", 203 and 210 each define an angle of approximately 60 degrees with respect to the longitudinal axis of the plunger or with respect to the adjacent side surface of an adjacent rib.

A resilient piston means is indicated generally byreference numeral 226 and is preferably formed of pharmaceutical or medical grade rubber or the like. This piston means includes a recess which is complementary to the reduced portion of the plunger and includes a taperedentry portion 222 for facilitating entry of the reduced portion thereinto.Tapered portion 222 joins with arecess portion 224 adapted to snugly receive the portion 2% of the reduced end of the plunger.

Arecess 226 formed within the piston means is adapted to receive theportion 202 of the plunger, and four spacedrecesses 230, 232, 234 236 are provided for receiving the four ribs formed on the plunger, each of the lastmentioned recesses being complementary to the ribs. It is apparent that when the reduced portion of the plunger is inserted in'the piston means, the piston means will move longitudinally with the plunger and cannot rotate with respect thereto in order to enable fine adjustments thereof.

The piston means is provided with a pair of peripherally extendingribs 240 and 244 formed on the outer surface thereof and adapted to engage the inner wall of the barrel. Rib 242 is provided with asharp edge 244 so as to provide good visual indication of the position of the piston within the transparent, or nearly transparent, barrel and to provide a good reading in cooperation with the indicia formed on the barrel.

A needle guard indicated generaly by reference numeral 256 is similar to the needle guard previously described and comprises an elongated hollow generally cylindrical main body portion 252 and an enlargedopen end portion 254 which is adapted to fit about the skirt and to have the terminal end thereof in abuting relationship with the adjacent end portion of the barrel. A peripherally extending sealing lip 256 is formed within theopen end portion 254 and is adapted to engage the outer surface of the skirt so as to retain the needle guard on the skirt and to provide a sterile seal with respect thereto.

When in the operative position as shown in FIG. 7, a shoulder 257 formed on the needle guard will abut up against the end surface of the skirt. A plurality of spaced longitudinally extendingribs 258 are provided on the outer surface of the needle guard to prevent rolling thereof along a supporting surface and to facilitate removal of the guard before use.

Opening means 268 is provided at the opposite end of the needle guard for aspirating air thereinto, a rib 262' being provided for maintaining a body of sterile filter material such ascotton 264 adjacent to theopening 260 to ensure that the air aspirated within the needle guard remain sterile.

It will be apparent that the operation and use of the disposably syringe illustrated in FIGS. 7 through 11 is substantially identical with that described in connection with FIGS. 1 through 6 inclusive, and in each case the device will remain sterile until used whereupon the boss portion of the barrel including the attached hypodermic needle may be broken away preferably by reinserting the needle guard in operative position and then bending it laterally so as to cause the frangible portion of the barrel to break away. It is apparent that once the boss and the needle have been broken away, the device is destroyed for any effective re-use thereof.

Referring now particularly to FIGS. 12 through 17, a further modified form of the disposable syringe according to the present invention is illustrated and which for example comprise a 10 cc. syringe. In this modification, a barrel includes amain body portion 270 having aradially extendingflange portion 272 provided at one end thereof terminating in aperipheral bead 274, the barrel being substantially cylindrical and hollow and with atapered entrance portion 276 to facilitate entry of the plunger thereinto. As in the previous modifications, the barrel in this modification is also formed of a material which is difficult to break such as polypropylene.

Aboss portion 280 extends longitudinally from thebarrel 270 and includes a taperedouter surface 282 which joins with a substantiallycylindrical surface 284 which in turn joins with abody portion 286 extending outwardly from the barrel and joined therewith by afrangible portion 288.Body portion 286 is provided with a plurality of angularly spaced and longitudinally extendingholes 287 to facilitate uniform cooling of the body portion and to prevent dimples from being formed therein.

As in the previously described modifications, thisfrangible portion 288 is defined between inner and outer surfaces of the barrel and is a thin walled annular portion of appreciably less thickness than the wall thicknesses at either side thereof. This frangible area is formed by a pair of annular shoulders 29% and 292 formed on the outer and inner surfaces of the barrel respectively and spaced longitudinally with respect to the barrel. These annular shoulders each define angles of substantially 90 degrees with respect to the associated inner and outer surfaces as indicated by the angles a and b. The length of the stress area again is approximately the same as the thickness of the thin wall portion and not more than twice this dimension. The annularsurfaces defining shoulders 290 and 292 as Well as the intersecting inner and outer surfaces each define an angle of approximately 45 degrees with respect to a phantom line MM drawn through the closest points on theinternal corners 294 and 2% formed at the outer and inner surfaces respectively.

A peripherally extending cutout portion 30% defining a substantially right angle is provided around the end of the barrel, this cutout being provided for facilitating removal of the barrel from its mold during themanufacturing process.

Theinner end wall 302 of the barrel is of generally concave configuration and has acentral recess 364 formed therein which in turn is in communication with a taperedportion 308 which is in communication with a longitudinally extending bore 310 formed through the central portion of boss 28%. The cooperation of the concave shaped innerend wall portion 362 and the tapered portion 368 is such as to assure that substantially all of the medicament is expelled from the barrel during operation of the apparatus.

The plunger means of this modification may be formed of a suitable substance such as polyethylene and includes an elongated substantially cylindricalhollow body portion 320 having spacedinternal ribs 322 formed thereon to rigidify the structure. Anenlarged end portion 324 is provided on the plunger for manual engagement, andexternal ribs 326 are formed on the outer surface of the plunger to strengthen the manually engaged end portion thereof.

The opposite end portion of the plunger includes a first reduced portion 30 having an outer four-sided symmetrical configuration with each of the sides flat and of substantially the same extent,portion 330 in turn joining with asecond portion 332 which is substantially cylindrical in configuration on its outer surface and which in turn joins with a slightlyenlarged portion 334 which also defines a cylindrical outer surface.

A resilient piston means is indicated generally byreference numeral 340, this piston means being formed of pharmaceutical or medical grade rubber or the like and having a recess formed therein complementary to the reduced end portion of the plunger. The recess in the piston means includes a first four-sided flat surfacedrecess 342 for snugly receiving theportion 330 of the plunger.

The recess also includes acylindrical portion 344 for snugly receiving theportion 332 of the plunger and a furthercylindrical recess portion 346 is adapted to snugly receive theportion 334 of the plunger. It is apparent that when the plunger is inserted in operative position within the recess in the piston means, the piston means will be mounted for movement with the plunger and at the same time cannot rotate with respect thereto so as to enable accurate and fine adjustment of the apparatus.

The piston means is provided with a pair of peripherally extendingribs 348 and 350 on the outer surface thereof for engaging the inner wall of the barrel.Rib 350 is provided with asharp edge portion 352 for providing accurate readings in combination with suitable indicia provided on thetransparent barrel portion 270.

The piston means is provided with anouter end wall 354 of generally concave configuration which is substantially complementary to that of theinner end wall 302 of the barrel when the plunger is moved into its innermost position as shown in FIG. 12 such that the piston means will fit snugly up against the inner wall of the plunger thereby assuring that substantially all of the medicament is expelled from the barrel.

A space 35:) is provided between the bottom of the recess formed in the resilient piston means 340 and the outerend Wall portion 357 of the reduced end of the plunger. This space enables the end of the piston to be deformed into the position shown in FIG. 12 wherein the space is flattened out and the ribs formed on the outer surface of the piston means are pressed firmly into engagement with the inner wall of the barrel. This flattening out of the piston means is caused by the hydraulic forces generated within the apparatus during operation.

Referring now particularly to FIG. 17 of the drawings, an arrangement is shown wherein the syringe may be sold and shipped without a hypodermic needle attached thereto. In such a case, it is desirable to provide a sterile package, and for this purpose an adaptor cap indicated generally by reference numeral 369 is provided. This adaptor cap comprises a generally cup-shaped hollow body portion formed of polyethylene or the like having anopen end 362 which fits snugly about theskirt 286 of the barrel so as to form a sterile seal therewith. The adaptor cap is provided with a plurality of spaced longitudinally extending reinforcingribs 364 on the outer surface thereof. It is apparent that after the syringe assembly has been shipped with the adaptor cap in place, it is merely necessary to slip the adapter cap off of the skirt and insert a hypodermic needle in position on the boss portion wherein the apparatus is ready for use.

A needle guard is illustrated in FIG. 12 and is indicated byreference numeral 370, this needle guard including anopen end portion 372 adapted to fit about theskirt 286. Theopen end portion 372 is provided with an inner peripherally extending rib 374 adapted to snugly engage the outer surface ofskirt 286 to retain the needle guard in operative position and to provide a sterile seal therewith.

As in the previous modifications,needle guard 370 is of hollow elongated configuration so as to enclose the hypodermic needle and to be spaced therefrom. The opposite closed end of the needle guard is provided with opening means 376 through which air is adapted to be aspirated. Arib 378 serves to hold a body of sterileabsorbent cotton 380 in place adjacent to the opening means 376 so as to filter any air aspirated into the needle guard and to retain the interior of the needle guard in a sterile condition.

The hypodermic needle in this particular modification may be identical with that previously discussed having a hub portion 382 which fits on theboss 280 so as to be snugly retained thereon by the outer taperedsurface 282 thereof, the needle including an elongatedhollow portion 384 which terminates in a sharpened point 386.

Referring now particularly to FIGS. 18 through 23 inelusive, a modified form of a disposable syringe is illustrated including a barrel 3% formed of a material such as polypropylene which is of hollow elongate configuration and which is generally cylindrical and includes an outwardly extendingcircumferential fiange 392 formed at the open end thereof and having a bead 394 formed at the periphery thereof. A tapered entrance portion 3% is provided for facilitating entry of the plunger.

A longitudinally extendingboss 397 extends from the opposite end of the barrel and includes a taperedouter surface 398 which joins with a substantiallycylindrical surface 399. This cylindrical surface in turn joins with an enlarged body portion 4% formed integral with the barrel and having a plurality of spacedholes 401 formed therein to facilitate more uniform shrinkage and to prevent dimples being formed in the plastic. The boss and body portion are joined with the main barrel portion by afrangible portion 402 extending annularly about the apparatus.

As in the previous modifications, the frangible portion is provided with built-in internal stresses in the manner aforedescribed, the frangible portion being formed by providing a firstannular shoulder 404 on the outer surface of the barrel and a second annular shoulder 4% formed on the inn-er surface of the barrel. As in the previous modifications, theshoulders 4434 and 406 define angles a and b of substantially 90 degrees with respect to the associated outer and inner surfaces respectively.

A phantom line NN has been drawn between the closest points on the internal corners as indicated byreference numerals 408 and 410 defined by the outer and inner shoulders respectively. The thickness .of the wall portion of the frangible area is appreciably less in thickness than the normal thickness of the adjacent wall portions at either side thereof, it being noted especially as seen in FIG. 20 that the holes 491 at widely spaced points do not interfere with this relationship. The longitudinal extent of the stress area is again approximately the same as the thickness of the frangible wall and not more than twice such dimension. The surfaces defining theannular shoulders 404 and 406 as well as the inner and outer sur-- faces intersecting these shoulder surfaces define an angle of approximately 45 degrees with respect to the line NN. Here again, this interrelationship creates such stresses in the material that it can be readily broken with manual effort.

Theinner end wall 412 of the barrel is of generally concave configuration and may define a portion of a spherical surface. This inner end wall has acentral recess 414 formed therein which in turn is in communication with a taperedportion 416 which joins with thebore 418 formed through the boss portion. Here again, the cooperation of the concave inner end wall portion along with therecess 414 and the taperedportion 416 ensures that substantially all of the medicament will be expelled from the barrel during operation.

The plunger of this particular modification may also be formed of polyethylene or similar substance and includes an elongatedhollow body portion 420 having three peripherally extendinginternal ridges 421, 422 and 423 formed thereon and spaced longitudinally thereof, these internal ridges facilitating removal of the plunger from the mold cavity during manufacturing. The open end of the plunger is provided with an outwardly extendingperipheral flange 425 adapted to be manually engaged, and a plurality .of reinforcingribs 426 are provided on the outer surface thereof.

.As seen particularly in FIG. 20, the opposite end of theplunger 420 is indicated byreference numeral 428 and as of reduced dimension, this reduced end portion including a longitudinally extendingshank portion 434 which is interconnected with a disc likeportion 432. Four spaced similar ribs extend outwardly fromportion 432, three of these ribs being visible in FIG. 20 and being indicated byreference numerals 434, 435 and 436, it being apparent that a rib similar to 435 is provided on the opposite side of the apparatus and not visible in this particular view, all of the ribs being equidistantly spaced from one another. The outer surfaces of each of the ribs is substantially planar and defines an oblique angle with respect to the longitudinal axis of the plunger, the three outer surfaces visible in FIG. 20 being indicated byreference numerals 434', 435 and 436' respectively.

A resilient piston means is indicated generally by refer nce numeral 44% in FIG. 20 and is formed of a suitable material such as pharmaceutical or medical grade rubber, this resilient piston means having a recess formed therein complementary to the reduced end portion of the plunger. This recess includes atapered entrance portion 442 which joins with ahole 444 complementary to and adapted to snugly receive theportion 430 of the plunger.

Recess portion 444 is in turn in communication with arecess portion 446 which snugly receivesportion 432 of the plunger. Four spacedrecesses 448, three of which are visible in FIG. 20 are provided for snugly receiving each of the ribs provided at the out-er end of a reduced portion of the plunger.

It is apparent that the interrelationship of the reduced end of the plunger and the resilient piston means will be such as to cause the piston means to move longitudinally with the plunger and also to prevent relative rotation between the piston means and the plunger so as to enable accurate adjustments of the apparatus.

A pair of peripherally extending spacedribs 450 and 452 are provided on the outer surface of the piston and are adapted to engage the inner wall of the barrel. Therib 452 is provided with asharp edge 454 so as to provide a good reading in cooperation with theindicia 456 provided on the barrel as indicated in FIG. 23.

Theouter end surface 456 of the resilient piston means of this modification is also provided with a generally concave configuration which is substantially complementary with theinner end wall 412 of the barrel such that the outer end wall of the piston means is adapted to fit snugly against the inner end wall of the barrel to ensure that all of the medicament is expelled when the plunger is moved inwardly.

The hypodermic needle of this modification includes ahub portion 460 having an inner tapered surface substantially complementary to the outer tapered surface of the hub so that the needle will be retained in place on the hub. The hypodermic needle also includes an elongatedhollow portion 462 terminating in asharp point 464. The needle hub may be knurled and formed of an aluminum alloy while theportion 462 thereof is preferably formed of stainless steel.

A needle guard is indicated generally byreference numeral 466 and includes anopen end portion 468 having a peripherally extendinginternal rib 470 which engages theouter surface 399 of the boss for engaging the outer surface of theskirt portion 400 of the barrel for retaining the needle guard in position on the skirt and for providing a sterile seal therewith. The opposite end of the needle guard is provided with opening means 472 through which air may be aspirated, and arib 474 is provided within the needle guard for retaining abody 476 of sterile cotton or other filter means in position adjacent the opening means 472 for filtering any air which may enter within the needle guard and for retaining a sterile atmosphere therewithin.

Referring now particularly to FIGS. 24 through 29 inclusive, there is illustrated a first modification of a sterile disposable needle container for shipping hypodermic needles. This container includes a body means indicated generally byreference numeral 480 and formed of a material such as polypropylene, and an enclosure means indicated generally byreference numeral 482 is formed of a material such as linear polyethylene which is a soft plastic which will not damage the sharp needle point should the point accidentally contact a portion of the enclosure means.

The body means 480 includes a first substantiallycylindrical portion 484 defining anopen end portion 485,portion 484 having a plurality of spaced longitudinally extendingflutes 486 extending therearound to facilitate grasping of the body means. The body means also includes anintegral portion 488 of reduced diameter as compared toportion 484,portion 488 having a plurality of spaced longitudinally extendingflutes 490 formed therearound. The twoportions 484 and 488 of the body means are joined by afrangible portion 492 extending annularly about the body means.

Referring now particularly to FIG. 29, the details of construction of thefrangible portion 492 are more clearly illustrated. As seen in this figure, the frangible portion comprises a pie-stressed area formed by providing a firstannularly extending shoulder 500 on the outer surface of the body means and a second annularly extending shoulder 502 formed on the inner surface of the body means. These two surfaces are offset with respect to one another longitudinally of the body means and define angles of substantially 90 degrees with the associated intersecting outer and inner surfaces respectively.

As in the previous modifications of the invention, the wall thickness of the frangible portion is appreciably less than that of the normal thickness of the adjacent wall portions. The length of the stress area is approximately the same as the thickness of the wall and under no circumstances more than twice the thickness of the wall. A phantom line OO has been drawn through the nearest points on theinternal corners 504 and 506 as defined respectively by intersection of the annular shoulders with the outer and inner surfaces of the body means. The surfaces defining the annular shoulders as well as the inner and outer surfaces each define an angle of approximately 45 degrees with respect to line OO. As in the previous modifications, this particular construction provides an arrangement whereby the frangible portion may be readily broken by hand.

The upper closed end of the body means as seen in FIGS. 26 and 27 is provided with four spacedinternal ribs 510 which extend radially inwardly of the portion 438 of the body means and extend longitudinally thereof. The purpose of these ribs will be hereinafter de scribed.

Abeveled edge 512 is provided around the body means just below the frangible portion as seen in FIGS. 24 and 26 and suitable printing is provided on this surface indicating that the body means is to be bent at that particular point so as to break away the upper reduced portion 483 of the body means. The body means is shown as being intact in FIG. 24 and as seen in FIG. 25, the frangible portion has been broken so as to leave anuneven edge 514, theportion 488 thereby being removed to expose a hypodermic needle indicated generally byreference numeral 516 which is disposed within the container.

The dimensions of theupper portion 488 are such as to permit theportion 488 to be bent to one side and to pivot over the end of the hypodermic needle without contacting the needle. In other words, as seen in FIG. 26 if lateral force were applied to the left hand side of theportion 488 as seen, the left hand portion of the frangible area would be the first to break and the part 4-83 would tend to pivot about the frangible portion as seen at the right of FIG. 26 with theportion 488 clearing the upper edge of the hypodermic needle so as to not interfere with the needle in any respect.

The loweropen end 485 of the body means is provided with abeveled entrance portion 52% to facilitate movement of the body means over the telescoping end portion of the enclosure means as hereinafter described. A peripherally extendinggroove 522 is provided in the inner surface of the lower open end portion of the body means and is provided with opposite sloping side surfaces 524 and 526.

The loweropen end portion 485 of the body means is also provided with four longitudinally extending slots spaced substantially degrees from one another. These slots are provided for the purpose of obtaining a certain degree of resilience at the lower open end of the body means such that it can be slightly expanded so as to be moved into the operative position shown in FIG. 26 as will be clear from the following description.

The enclosure means 4S2 includes a main elongatedhollow body portion 530 which is normally disposed in spaced relationship to the enclosed hypodermic needle and which includes a lowerclosed end portion 531. Four longitudinally extendingribs 532 are formed on the outer surface ofportion 530. Theseribs 532 are disposed substantially 90 degrees apart and are adapted to fit within the slots formed in the lower open end portion of the body means when the twoportions 480 and 482 of the container are snapped into operative position as shown in FIG. 26.

The upper portion of the enclosure means as seen in FIG. 26 is provided with a peripherally radially outwardly extending attachingshoulder 536 having opposite sloping side surfaces 538 and 540. This attaching shoulder is adapted to fit snugly within thegroove 522 provided in the body means, and when the twoportions 482 and 436 have been snapped into the telescopic relation shown in FIG. 26, the two members will be locked together and cannot be removed simply by applying effort to pull them apart longitudinally. It is apparent that thebeveled entrance portion 520 will facilitate movement of the parts into the assembled relation shown as will the slottedopen end portion 485 of the body means.

The upper portion of the enclosure means is also provided with a peripherally extending sealingrib 542 formed on the outer surface thereof which is adapted to engage the adjacent inner surface of theportion 484 of the body means so as to provide a sterile seal therewith.

It will also be noted that the uppermost open end of the enclosure means is provided with abeveled portion 544 which is adapted to cooperate with thebeveled portion 520 formed on the body means for facilitating entry of the enclosure means into the body means.

The enclosure means includes acentral bore 546 for receiving the main part of the hypodermic needle, and a hexagonal socket portion 543 is provided at the open upper end thereof for snugly receiving a correspondingly shaped portion of the hub of the needle. The thickened upper portion of the enclosure means is provided with a plurality-of spaced longitudinally extendingholes 550 formed about the central bore therethrough, these holes serving to ensure more uniform cooling of this portion of the enclosure means and to prevent dimpling thereof.

The hypodermic needle includes a hub of an anodized aluminum alloy and anelongated portion 554 formed of stainless steel.

When assembling the container as shown in FIG. 26, theportions 480 and 482 are initially separate from one another and the hypodermic needle will be inserted in operative position in thesocket portion 548 of the enclosure means as shown.

The body means 480 will then be moved into telescoping relationship with the upper end of the enclosure means until theshoulder 536 on the enclosure means snaps into thegroove 522 provided in the body means, and with the upper end of theribs 532 of the enclosure means fitting within theslots 528 of the body means.

The body means is formed of polypropylene and is sufficiently resilient to be snapped into the operative position shown in FIG. 26, but it cannot be pulled back to off. With this arrangement, the container is tamperproof since it must be broken or destroyed in order to open the container. In addition, this permanent attachment of the body means to the enclosure means is an important consideration in obtaining and retaining a sterile condition within the container. After the members have been snapped into position as shown, a closed capsule or 17 housing is provided which is adapted to retain sterilizing gas as hereafter described. Accordingly, the hypodermic needle is maintained in a sterile condition and further is protected from damage during shipment and up until the time it is actually desired to be used.

When the body means 480 is pushed into the operative position as shown in FIG. 26, theribs 510 will tend to move the hypodermic needle downwardly as seen in FIG. 26 by engaging the upper surface thereof so as to ensure that the needle is properly seated within the enclosure means socket. Additionally, these ribs will prevent the needle from coming out of the socket in the enclosure means and thereby serve to retain the needle in its proper operative position within the container.

When sterilizing this package or container with the needle therein, the whole package is placed within a chamber which is evacuated to an equivalent to 14 p.s.i. negative pressure which pulls out the original air in the package. The chamber is then pressurized up to 20 p.s.i. with a sterilizing gas as mentioned hereinbefore whereby the entire assembly is automatically filled with the sterilizing gas. Even if the ethylene oxide escapes by penetrating through the plastic walls of the container until the internal pressure is equalized with the outside atmospheric pressure, the carbon dioxide which will not penetrate the Walls remains within the container and is eX- tremely inert and does not support bacterial growth. The sealingring 542 will hold from 3 to p.s.i. within the package, and accordingly, it is apparent that an inert gas will be trapped within the container to maintain sterility control. This same feature is also incorporated in the modification illustrated in FIGS. 30 and 31.

Referring now to FIGS. 30 and 31, modified forms of the body means and enclosure means are illustrated respectively. It is apparent that these two portions are adapted to be snapped into operative position as are theportions 480 and 482 respectively for retaining a hypodermic needle therein.

Referring now particularly to FIG. 30, a modified form of the body means is illustrated including a first substan tiallycylindrical portion 560 having a plurality of spaced longitudinally extendingflutes 562 formed in the outer surface thereof for facilitating grasping thereof. Theopen end portion 563 of the body means is provided with a laterally extendingflange portion 564 which is provided with flats on the outer surface thereof to prevent rolling of the body means and the attached enclosure means along a supporting surface. This provision of the flats on the body means further ensures the prevention of rolling, the ribs formed on the enclosure means of both of the modifications of the needle container also serving this same function.

The body means shown in FIG. 30 also includes aportion 566 of reduced diameter having a plurality of spaced longitudinally flutes 568 formed on the outer surface thereof. Reducedportion 566 is interconnected withportion 560 by means of a frangible portion indicated generally by reference numeral 57 0.

The body means of this modification is also formed of polypropylene and thefrangible portion 570 is provided with the desired characteristics by providing a particular construction so as to render it readily breakable with manual effort.

A pair ofannular shoulders 572 and 574 are provided on the outer and inner surfaces of the body means respectively and are offset or spaced from one another longitudinally of the body means. Each of these annular shoulders defines an angle of approximately 90 degrees with the intersecting associated outer and inner surfaces respectively. These angles are indicated by the letters a and b respectively.

A phantom line PP has been drawn through the nearest points on theinternal corners 576 and 578 defined by the intersection of the annular shoulders with the outer and inner surfaces of the body means.

The thickness of the wall of the frangible portion is again appreciably less than the normal thickness of the Walls at either side thereof, and the length of the stress area should be approximately the same as the thickness of the wall and not more than twice such dimension. The annularsurfaces defining shoulders 572 and 574 as well as the adjacent intersecting inner and outer surfaces each define an angle of approximately 45 degrees with respect to the phantom line PP. With this over-all arrangement, the frangible area is again rendered readily breakable by manual efr'ort when lateral forces are applied to the body means outer closed end portion. As in the previous needle container, this end portion of the body means which is broken away is so designed and related to the upper end of the hypodermic needle that it will pivot over the needle without touching or interfering with the needle when it is broken away.

The upper closed end of the body means is provided with a plurality of ribs 580 which extend radially inwardly from the inner wall thereof and which extend longitudinally of the body means. These ribs serve the same purpose as theribs 510 discussed in connection with the pre vious modification for moving the hypodermic needle in its proper operative position and for retaining it in such position until used.

Abeveled surface 582 extends peripherally about the body means and may be provided with suitable printing thereon to indicate that the body means is to be broken adjacent such point in order to open the container.

The open end of the body means is provided with abeveled entrance portion 584 which may be beveled at an angle of approximately 30 degrees with the respective inner surface of the body means so as to facilitate entry of the enclosure means thereinto as will be well understood.

A peripherally extendinginternal groove 586 is provided within the body means and is provided with opposite sloping side surfaces 588 and 590, this groove being adapted to receive the attaching shoulder provided on the enclosure means hereinafter described.

In this particular modification, the body means is not provided with any longitudinally extending slots as is the previously described modification, and the enclosure means is simply forced into position within the body means utilizing the natural resilience of the plastic parts.

Referring now particularly to FIG. 31 of the drawings, a modified form of the enclosure means is illustrated which includes a main elongated hollow body portion 600 which may be for-med of a material such as linear polyethylene. This body portion has aclosed end 602 and an openopposite end portion 604. A plurality of spacedribs 606 are provided on the outer portion of body 600, the ribs preferably being'four in number and equally spaced from one another although any desired number of ribs may be employed. In this particular modification, the ribs terminate at thepoint 610 and do not extend into any slot portions formed in the body means since in this particular case the body means is not provided with any slots for receiving the ribs.

A peripherally extending sealingrib 612 is formed on the outer surface of theopen end portion 604 of the enclosure means, this rib being adapted to engage the inner surface of the body means so as to provide a sterile seal therewith in the same manner in whichrib 542 on the enclosure means illustrated in FIG. 26 provides a sterile seal with its associated body means.

' A peripherally extending attachingshoulder 614 is pro vided on the outer surface of the enclosure means and is provided with afirst side surface 616 and a secondsloping side surface 618. It will be noted that theside surface 616 forms an angle of approximately degrees with the associated outer surface of the enclosure means while thesurface 618 slopes at an oblique angle to the same outer surface.

As in the previously described modification of the 19 needle container, the attachingshoulder 614 is adapted to snap into place within theinternal groove 586 provided in the body means so that the body means and its associated enclosure means when in telescoping arrangement cannot be separated from one another without destroying the package. Thesurface 616 being formed at right angles to the outer surface additionally ensures that it will be even more difiicult to remove the body means from the enclosure means, and accordingly the only manner in which the enclosed hypodermic needle can be removed is by breaking away the body means thereby preventing re-use of the container and making the container tamper-proof.

The enclosure means is provided with acentral boss 620 which receives the tubular portion of the hypodermic needle, and ahexagonal socket 622 is provided for receiving a correspondingly shaped portion of the hub of the needle. A plurality of spaced longitudinally extendingholes 624 are provided in surrounding relationship to the bore within the enclosure means, these holes serving to ensure substantially uniform cooling of the enclosure means and to prevent dimpling thereof.

In each modification of the needle container means, a beveled inner edge is provided in the body means for facilitating sliding of the enclosure means thereinto. Also in each modification, the side surface of the attaching shoulder closest to the open end of the enclosure means is provided with a sloping configuration so as to cooperate with the inner beveled edge on the body means to cam the open end of the body means over such attaching shoulder and to permit the attaching shoulder to snap into operative position as aforedescribed.

In each modification of the needle container means, the closed end of the body means may be provided with any suitable identification in the form of printing or embossments to identify the particular type of hypodermic needle carried within the container.

It will of course be realized that the. modification illustrated in FIGS. 30 and 31 when in assembled relationship can be sterilized in the same manner as discussed in connection with the modification shown in FIGS. 2429, and furthermore theportion 566 of the body means shown in FIG. 30 can be broken off along the annularfrangible portion 570 and pivoted in such a manner as not to interfere with or contact a hypodermic needle disposed within the container.

Referring now to FIG. 32 of the drawings, a modification of the disposable syringe mechanism isillustrated wherein theboss 630 may be similar to the bosses provided on the different barrels of the various modifications of the invention, it being understood that this particular modification can be incorporated with different ones of the disposable syringe modifications as previously described.

Theboss portion 630 is interconnected by means of a frangible portion indicated generally by reference numeral 632 with the main body portion of the barrel as will be well understood from a description of the previous modifications. Theboss portion 630 is provided with a tapered outer surface 634 as previously described which is complementary to aninternal taper 636 formed on thehub portion 638 of a hypodermic needle indicated generally byreference numeral 640.

As pointed out previously, this type of taper in the hub portion of the hypodermic needle is known as a Luer taper, but it has been found that even though the boss portion may be pressed quite tightly within the hub portion of a needle of this type, the needle will eventually become loose because of the tendency of the polypropylene material of the boss portion to conform or cold flow to the contour of the hub of the needle whereupon the holding power or resistance to movement is lost.

As in the previous modifications, theboss portion 630 is provided with aninternal bore 642 which joins with a taperedportion 644 which in turn connects with arecess portion 646 formed in the centralpart of the end wall of the barrel as previously discussed.

A skirt portion indicated by reference numeral 650 is disposed in surrounding spaced relationship to theboss portion 630 and is disposed in surrounding relation to a part of the tapered portion of the .boss. It will be noted that ashort portion 630 of the boss defines a cylindrical surface which in turn joins with the tapered outer surface 634 at a point indicated byreference numeral 635.

The end of the skirit portion includes a tapered entrance area 652 the tapered surface of which facilitates entry of the end portion of the hub within the skirit means as will be apparent.

The skirt portion also includes anannular shoulder portion 654 which extends peripherally around the interior of the skirt portion and projects inwardly therefrom. This shoulder defines an angle with a line drawn parallel with the longitudinal axis of the body means which is indicated by the letter 12 in the drawing, this angle being approximately 60 degrees.

The terminal end of thehub portion 638 of the hypodermic needle includes anenlarged portion 660 having an annularperipherally extending shoulder 662 formed thereon. As seen in FIG. 32, this shoulder is so arranged as to abut snugly against theshoulder 654 formed on the skirt portion.

It is apparent that when the hypodermic needle is assembled in operative position within the skirt portion as shown in FIG. 32, the needle hub will be adapted to snap into the position shown whereupon the cooperation ofshoulders 654 and 662 will prevent withdrawal of the hub from the body means of the syringe. The hub thereby snaps in place and is permanently held and cannot be removed or withdrawn.

It is apparent from the foregoing that there is provided according to the present invention a new and novel disposable sterile device which remains a sterile package until used and Which is adapted to be used only one time and then thrown away and completely discarded. The device of each modification includes means for effectively destroying the device by breaking away a portion thereof to revent re-use for the intended purpose.

The disposable syringes of the present invention eliminate possible cross contamination, save the time of the operator and further are convenient and comfortable for the patient. These disposable syringes provide means for effectively filtrating the aspirated air drawn into the needle guards thereof and furthermore provide an arrangement which assures that substantially all of the medicament will be expelled from the syringes during operation. Each of the syringes is provided with resilient piston means having a very sharp line thereon to give accurate readings thereby indicating exact dosages in cooperation with the indicia provided on the barrels of the syringes. In each case, the resilient piston means is fixed to the associated plunger and cannot rotate with respect thereto which enables the plunger and piston means to be twisted as well as moved longitudinally within the barrel to obtain very fine adjustments.

In one modification of the adjustable syringe means, an auxiliary means is provided for holding a hypodermic needle in place in the form of a skirt disposed in surrounding relationship to the boss which supports the needle. In another modification of the invention, a unique arrangement is provided for enabling hydraulic pressure to urge the piston means outwardly such that the ribs on the outer surface thereof are pressed tightly against the inner surface of the associated barrel.

In each modification of the needle container means of the present invention, a tamper-proof arrangement is provided which necessitates the breaking away of a portion thereof so as to render the package in such a condition that it cannot be re-used for the intended purpose. Additionally, a sterile atmosphere. is retained within the needle container means until the body means thereof is broken.

As this invention may be embodied in several forms without departing from the spirit or essential characteristics thereof, the present embodiment is therefore illustrative and not restrictive, and since the scope of the invention is defined by the appended claims, all changes that fall within the metes and bounds of the claims or that form their functional as well as conjointly cooperative equivalents are therefore intended to be embraced by those claims.

I claim:

1. A disposable sterile medical and surgical device adapted to be used only one time and then discarded including a body means formed of polypropylene, said body means defining a hollow member open at one end thereof, said body means including an intermediate frangible portion for separating the body means into two separate pieces and for preventing effective re-use thereof, said frangible portion having internal stresses therein defining a prestressed area of relatively thin wall thickness which is appreciably less thick than the adjacent wall portions and which pre-stressed area can be readily broken with manual effort.

2. A disposable sterile medical and surgical device adapted to be utilized only once and then discarded comprising a body means formed of polypropylene, said body means defining a hollow member including a first portion and a second portion of reduced dimension as compared to said first portion, said first and second portions being interconnected by a frangible portion for separating said first and second portions completely from one another so as to prevent effective re-use of the device, said frangible portion including a pre-stressed area, said pre-stressed area being defined between the inner and outer surfaces of said body means and between a first laterally extending shoulder formed on the inner surface and a second laterally extending shoulder formed on the outer surface, said shoulders being offset with respect to one another and defining an angle of substantially 90 degrees with respect to the respective surfaces.

3. A disposable sterile medical and surgical device adapted to be used only once and then discarded, said device including a hollow body means formed of polypropylene, said body means including a first generally cylindrical portion and a second portion of reduced diameter extending longitudinally of said first portion, said first and second portions being interconnected by a frangible portion adapted to be broken and to separate the body means into two separate pieces to prevent effective re-use thereof, said frangible portion including an annular wall area which has a thickness appreciably less than the thickness of the adjacent wall portions, said wall area being internally pre-stressed so as to be readily broken by manual effort, said stresses in the frangible portion being concentrated between a first annular shoulder formed on the outer surface of the body means and a second annular shoulder formed on the inner surface of the body means, said shoulders being offset longitudinally of the body means with respect to one another and each extending at an angle of substantially 90 degrees to the respective outer and inner surfaces, there being defined sharp corners between the shoulders and the respective surfaces.

4. Apparatus as defined in claim 3 wherein each of said shoulders defines an angle of approximately 45 degrees with respect to a line drawn between the closest points on the internal corners of the shoulders as defined by the intersection of the shoulders and the respective surfaces.

5. Apparatus as defined in claim 3 wherein the longitudinal extent of the area of stress defined in the frangible portion is not more than two times the thickness of the wall area of the frangible portion.

6. A disposable sterile medical and surgical device comprising a hollow body means formed of organic plastic material of low molecular weight which is hard flowing and sets up quickly in a mold and is difficult to break,

said body means including an intermediate frangible portion for separating the body means into two separate pieces, so that the body means cannot be efiectively reused for its intended purpose, said frangible portion including a prestressed area having a concentration of stresses therein to render said area readily breakable by manual effort, and enclosure means disposed in telescoping relationship with said body means and being engaged therewith to define with the body means an enclosed space.

7. Apparatus as defined in claim 6 wherein said enclosure means includes a peripherally extending sealing means formed on one surface thereof in engagement with a surface of said body means for providing a sterile seal therewith.

8. A disposable sterile medical and surgical device adapted to be used one time and then discarded comprising a body means formed of polypropylene material which is normally difficult to break, said body means being hollow and open at one end thereof and including an intermediate frangible portion for separating the body means into two separate pieces to prevent effective re-use thereof for the intended purpose, said frangible portion including a prestressed area having a concentration of stresses therein, so as to render the frangible portion readily breakable by manual effort, an enclosure means including a hollow elongated body closed at one end thereof and having an open end, said last-mentioned end being telescopically engaged with said body means to define an enclosed space therewith, a hypodermic needle means supported within said enclosed space, and means to hold the hypodermic needle means in operative position within said space.

9. Apparatus as defined inclaim 8 wherein said enclosure means includes means formed at the open end thereof and engaging the adjacent body portion to provide a sterile seal therewith to retain -a sterile atmosphere within the enclosed space within which the needle means is disposed.

10. A disposable sterile medical and surgical device adapted to be used a single time and then discarded comprising a body means formed of polypropylene, said body means being of elongate hollow construction and open at one end thereof, said body means including an intermediate frangible portion for separating the body means into two separate pieces to prevent effective re-use thereof, said frangible portion defining a thin annular wall area of appreciably less thickness than the adjacent wall portions, said frangible portion including a pre-stressed area which enables the frangible portion to be readily broken by manual effort, the stresses within said frangible portion being defined between a first annular shoulder formed on the outer surface of the body means and a second annular shoulder formed on the inner surface of the body means, said shoulders being offset longitudinally with respect to one another and defining angles of substantially degrees to the respective surfaces, enclosure means including an elongated hollow body means open at one end thereof, the open end of said enclosure means being operatively associated with said body means so as to be in engagement therewith and to be supported thereby, means providing a sterile seal between said enclosure means and said body means in order to retain a sterile atmosphere within the enclosed space defined by said enclosure means and said body means, and a hypodermic needle means supported and carried by said body means and enclosure means as a unit, and means for retaining the needle means in operative position relative thereto.

11. Apparatus as defined inclaim 10 wherein each of the annular shoulders defines an angle of approximately 45 degrees with respect to a line drawn between the closest points of the internal corners as defined between the intersection of the shoulders with the respective surfaces.

12. Apparatus as defined in claim wherein the stress area of the frangible portion has a longitudinal dimension of not more than two times the thickness of the wall at the frangible stress portion.

13. A disposable syringe comprising an elongated hollow barrel formed of organic plastic material of low molecular weight which is hard flowing and sets up quickly in a mold and is normally diflicult to break, a boss extending longitudinally of said barrel and connected therewith, a plunger slidably mounted within said barrel, piston means mounted on the inner end of said plunger and engaging the inner wall of said barrel, said barrel including a frangible portion formed intermediate the main barrel portion and. said boss, said frangible portion defining a prestressed area wherein there exists a concentration of stresses to render the frangible portion readily breakable by manual effort, whereby said boss may be broken away from the main barrel portion to prevent the syringe from being re-used.

14. A disposable syringe adapted to be used one time and then discarded comprising an elongated hollow barrel formed of polypropylene, a boss extending longitudinally from one end of said barrel, said boss being of reduced cross sectional dimension as compared with said barrel, the boss being interconnected with said barrel by frangible portion, said frangible portion including an annular wall forming a pre-stressed area having a concentration of stresses therein which enables the frangible portion to be readily broken away, a plunger slidably positioned within said barrel, and resilient piston means mounted on one end of said plunger and engaging the inner wall of the barrel.

15. A disposable syringe comprising an elongated hollow barrel formed of polypropylene, a boss extending longitudinally from one end of said barrel and being connected with said barrel by means of a frangible portion, said frangible portion including an annular wall area, said Wall area having a thickness appreciably less than the adjacent wall portions of the barrel and the boss respectively, said frangible portion including a prestressed area having a concentration of stresses therein to render the frangible portion readily breakable by manual effort, whereby the boss may be broken away from the barrel so as to prevent re-use of the syringe, a plunger slidably positioned within said barrel and including a reduced end portion, piston means mounted on said reduced end portion, said piston means engaging the inner wall of said barrel, the reduced end portion of said plunger and said piston means including intercooperating means for preventing relative rotation between said piston means and said plunger means.

16. Apparatus as defined in claim wherein said piston means includes on the outer surface thereof a sharp edge to provide a means for obtaining a clear and accurate reading, said barrel being translucent and having indicia thereon to provide such reading.

17. Apparatus as defined inclaim 15 wherein the means for preventing relative rotation between said plunger and said piston means includes an irregular configuration formed on the reduced end of the plunger, said piston means having a complementary irregular recess formed therein which receives the irregular reduced end of the plunger.

18. Apparatus as defined inclaim 15 wherein a needle guard is mounted on the boss and is provided with means on the outer surface thereof to prevent rolling of said needle guard along a surface.

19. A disposable syringe comprising an elongated generally cylindrical and hollow barrel formed of polypropylene, said barrel being translucent and having the indicia formed thereon, a boss extending longitudinally of said barrel and being connected with said barrel by an intermediate fragible portion, said boss having a bore formed therethrough and the outer surface thereof being tapered, said barrel including an inner end wall which is substantially concave in configuration, the opposite end of said barrel being open, said fragible portion including an annular wall having a thickness appreciably less than the thickness of the adjacent wall portions on either side thereof, said thin wall portion including an internal prestressed area having a concentration of stresses formed therein so as to render the frangible area readily breakable with manual effort, an elongated plunger freely slidably mounted in said barrel and including an enlarged end portion at one end thereof to be manually engaged and having a reduced end portion at the opposite end thereof, said reduced end portion whereby when the reduced silient piston means mounted on said reduced end of the plunger, said piston means having an irregular recess formed therein complementary to the irregular shape of said reduced end portion whereby when the reduced end portion is received within said recess relative rotation between said piston means and said plunger is prevented, said piston means having an outer end portion which is of generally concave configuration and substantially complementary to the shape of the inner end wall of the barrel so as to provide a snug fit therewith and to assure that substantially all of the medicament is expelled from the barrel when the piston means is moved inwardly, said piston means having a pair of spaced annularly extending ribs formed on the outer surface thereof, the innermost of said ribs having a sharp edge thereon to give a good reading in cooperation with the indicia formed on said barrel, a hypodermic needle including a hub portion and a hollow elongated portion terminating in a sharp point, said hub portion being mounted on the tapered outer surface of said boss, and a needle guard disposed in surrounding enclosing relationship with said needle, said needle guard having an open end portion mounted on a portion of said barrel and including an annularly extending sealing means formed on the inner surface thereof and in contact with said barrel portion to provide a sterile seal therewith.

20. Apparatus as defined inclaim 19 wherein said frangible pre-stressed area is defined between inner and outer surfaces of said barrel and is developed by a pair of annular shoulders each of which intersects one of said surfaces at an angle of substantially degrees to define a sharp corner therewith, said shoulders being spaced longitudinally of one another.

21. A disposable syringe comprising an elongated generally cylindrical hollow barrel of polypropylene, a boss extending longitudinally from one end portion of said barrel and being adapted to receive a hypodermic needle and support such needle, said boss being connected with said barrel by a frangible portion, said frangible portion including an annular wall of appreciably less thickness than the adjacent wall portions at either sides thereof, said frangible portion defining a pre-stressed area having a concentration of stresses therein which renders the trangible area readily breakable by manual effort, a plunger slidably positioned within said barrel, said plunger including a reduced end portion which is bifurcated to define a pair of spaced portions having tapered side surfaces which are disposed at an oblique angle to the longitudinal axis of said plunger, resilient piston means having recess means formed therein complementary to the reduced end portion of the plunger so as to receive such reduced end portion and to prevent relative rotation between the plunger and piston means thereby enabling fine adjustment of the plunger and associated piston means relative to the barrel.

22. A disposable syringe comprising an elongated hollow barrel formed of polypropylene material which is normally difficult to break, a boss extending longitudinally of said barrel and being of reduced cross sectional dimension, said boss being interconnected with said barrel by means of a frangible portion, said frangible portion comprising a thin wall area of appreciably less thickness than the adjacent Wall portions on either side thereof,

said thin wall area being internally prestressed and having a concentration of stresses therein so as to render the frangible area readily breakable by manual effort, a skirt portion formed integral with said barrel and extending longitudinally thereof and being disposed in spaced surrounding relationship to a portion of said boss, a plunger slidably positioned within said barrel, said plunger having an enlarged portion formed at one end thereof and adapted to be manually engaged and including a reduced end portion at the opposite end thereof, said reduced end portion defining a plurality of spaced ribs, resilient piston means mounted on the reduced end of said plunger and engaging the inner wall of said barrel, said piston means including a recess complementary to the shape of the reduced end portion of said plunger for receiving such reduced end portion and for securing the piston means in operative position and preventing relative rotation between the piston means and the plunger.

23. Apparatus as defined inclaim 22 wherein said ribs formed on the reduced end portion of said plunger are angularly spaced with respect to one another and define flat side surfaces lying generally in planes parallel with the longitudinal axis of said plunger, said ribs also including sloping outer edge portions disposed at an angle to the longitudinal axis of the plunger.

24. Apparatus as defined in claim 23 wherein each of said ribs includes a first outer edge portion defining an angle of approximately 60 degrees with respect to the flat side surface of an adjacent rib and also including a second outer edge surface which defines an angle of approximately 20 degrees with respect to a plane passing through the fiat side surface of an adjacent rib.

25. Apparatus as defined inclaim 22 wherein said boss is provided with a tapered outer surface, a hypodermic needle having a hub portion seated on the tapered surface of said boss and fitting between said boss and said skirt portion and engaging said skirt portion for retaining the hypodermic needle in position.

' 26. Apparatus as defined inclaim 22 including an elongated hollow needle guard having an open end portion, said open end portion being disposed in surrounding relationship to said skirt, said open end portion including a radially inwardly extending sealing means engaged with said skirt portion for retaining said needle guard on said skirt portion and for providing a sterile seal therewith.

27. A disposable syringe comprising an elongated hollow barrel formed of polypropylene material which is normally difficult to break, a boss extending longitudinally of said barrel and interconnected therewith by a frangible portion, said frangible portion including a prestressed thin wall area of appreciably less thickness than the adjacent wall portions on either side thereof, said thin wall area including built-in concentrated internal stresses to render the frangible area readily breakable under manual pressure, said boss including a first substantially cylindrical portion of constant diameter joining with a tapered portion which tapers inwardly toward the outer end of the boss, an integral body portion extending from said barrel in surrounding relationship to a portion of said cylindrical part of the boss and having a plurality of spaced holes formed therein, a plunger slidably positioned within said barrel, said plunger including a first enlarged end portion adapted to be manually engaged and a second opposite reduced end portion, piston means formed of resilient material and mounted on said reduced end portion, the reduced end portion of said plunger having a non-circular configuration and said piston means having a recess of complementary configuration such that when the piston means is mounted on the plunger relative rotation therebetween is prevented.

28. A disposable syringe comprising a barrel of a generally cylindrical hollow configuration and formed of polypropylene, a boss extending longitudinally of said barrel for receiving a hypodermic needle and being interconnected with said barrel by a frangible portion, said frangible portion including an annular thin wall prestressed 'area of appreciably less thickness than the adjacent wall areas at either side thereof, said thin wall area including a concentration of stress therein so as to be readily broken with manual effort, a plunger slidably positioned within said barrel, said plunger having a first enlarged end portion adapted to be manually engaged and including an opposite reduced end portion, resilient piston means mounted on said reduced end portion, said.

reduced end portion including a part having a non-circular configuration, said piston means having a recess of complementary configuration for receiving the reduced end portion of the plunger and for preventing relative rotation between the plunger and the piston means, and there being a free space between the end of said plunger and the bottom of the recess within said piston means to enable the piston means to be flattened out under the force of hydraulic pressure when the apparatus is being operated.

29. A needle container comprising a body means formed of organic plastic material of low molecular weight which is hard flowing 'and sets up quickly in a mold and is normally difficult to break, said body means being elongated and hollow and open at one end thereof, an enclosure means telescopically fitted with said body means, said enclosure means being hollow and including an open end, a hypodermic needle supported therein, means for locking said body means and said enclosure means to one another to prevent them from being separated, and said body means including an intermediate frangible portion, said frangible portion including a prestressed area having a concentration of stresses therein 'and comprising an annular thin wall area of appreciably less thickness than the adjacent wall areas at either side thereof, to enable the frangible portion to be readily broken by manual effort.

30. Apparatus as defined in claim 29 including means defining a sterile seal between said body means and said enclosure means so as to effectively entrap a sterile atmosphere within the hollow space defined by the body means and the enclosure means.

31. Apparatus as defined in claim 29 wherein said body means as a closed end portion opposite to the open end portion thereof, and rib means formed on the inner surface of said body means adjacent said closed end thereof and extending radially inwardly of the inner surface of the body means.

32. Apparatus as defined in claim 29 wherein said body means has formed in the walls thereof adjacent the open end thereof spaced slots for providing resilience to said body means.

33. Apparatus as defined in claim 32 wherein said enclosure means has formed on the outer surface thereof spaced rib means, said last-mentioned rib means being adapted to fit within the slot means formed in said body means.

34. A needle container comprising a body means formed of polypropylene, said body means being hollow and closed at one end thereof and open at the opposite end thereof, said body means having a peripheral groove formed in the inner surface thereof, said groove including sloping side surfaces, said body means also including an inner beveled edge formed at the open end thereof, enclosure means fitting within said body means in telescopic relationship, said enclosure means being hollow and including an open end for receiving a hypodermic needle and an opposite closed end, said enclosure means having a peripherally extending shoulder formed on the outer surface thereof with sloping side surfaces and adapted to fit relatively snugly within the groove formed in said body means for locking the enclosure means and body means together and for preventing separation thereof once they have been moved into operative position, and sealing means defining a sterile seal between said enclosure means and said body means to entrap a sterile atmosphere in the hollow space defined by said body means and said enclosure means, said body means including an intermediate frangible portion, said frangible portion comprising a thin walled area of appreciably less thickness than the adjacent wall areas at either side thereof, said thin wall area including the concentration of stress within the material of the body means so as to render the frangible portion readily breakable with manual effort.

35. Apparatus as defined in claim 34 wherein said enclosure means has a plurality of holes disposed therein adjacent the open end thereof and in surrounding relationship to the opening formed in the open end thereof.

36. A needle container comprising a body means formed of polypropylene, said body means being hollow with a closed end and an open end, said body means having an inner peripheral groove formed therein, said groove having sloping side surfaces, said body means also including an inner beveled edge formed at the open end thereof, said body means having radially inwardly extending rib means formed on the inner surface thereof adjacent the closed end of the body means, enclosure means fitting telescopically within said body means and being hollow and having an open end and a closed end, said open end fitting within said body means and being adapted to receive a hypodermic nedle disposed within the hollow space defined between said body means and said enclosure means, said enclosure means having a peripherally extending shoulder formed on the outer surface thereof and fitting within the peripheral groove formed within said body means, said shoulder having a first sloping side surface nearest to the open end of the enclosure means and a second side surface extending substantially perpendicularly to the associated side surface of the enclosure means, whereby the enclosure means and the body means cannot be readily separated when in assembled relationship with said shoulder disposed within said groove, and said body means having an intermediate frangible portion, said frangible portion including a prestressed area having a concentration of stresses therein and comprising an annular thin wall portion of appreciably less thickness than the wall portions at either side thereof which renders the frangible portion readily breakable.

37. Apparatus as defined in claim 36 wherein said enclosure means has a plurality of outwardly extending spaced ribs formed on the outer surface thereof, said ribs terminating at a point adjacent the open end of said body means when the body means and enclosure means are in assembled operative relationship.

38. A disposable sterile device adapted to be utilized only once and then discarded comprising a body means formed of polypropylene, said body means defining a hollow member including a first portion and a second portion of reduced dimension as compared to said first portion, said first and second portions being interconnected by a frangible portion for separating said first and second portions completely from one another so as to prevent effective re-use of the device, said frangible portion including a pre-stressed area having a concentration of stresses therein which can be readily broken with manual effort, said second portion of reduced dimension including an outer tapered surface portion, a

skirt means disposed in spaced surface portion, a skirt means disposed in spaced surrounding relationship to a portion of said tapered portion, a hypodermic needle having a hub portion, said hub portion having an internal taper complementary to the taper formed on said second portion of the body means, said hub of the needle being snugly received on said tapered portion of the body means and the terminal end of said hub portion being disposed within said skirt means, said skirt means including a peripherally extending shoulder formed thereon and projecting inwardly thereof, said hub including a shoulder portion in engagement with the shoulder portion on said skirt means to securely attach the hub portion of the needle to said body means.

39. Apparatus as defined in claim 38 wherein said skirt means includes a tapered entrance portion to facilitate movement of a needle hub into the skirt means.

40. Apparatus as defined in claim 38 wherein said shoulders formed on said skirt means and said needle hub define an angle of approximately degrees with respect to a line drawn parallel with the longitudinal axis of said body means.

41. A disposable syringe comprising an elongated hollow barrel formed of polypropylene material which is normally difficult to break, a boss extending longitudinally of said barrel and being of reduced cross sectional dimension, said boss having a tapered outer surface and being interconnected with said barrel by means of a frangible portion, said frangible portion comprising a thin wall area of appreciably less thickness than the adjacent wall portions on either side thereof, said thin wall area being internally pre-stressed and including a concentration of stresses therein so as to render the frangible area readily breakable by manual effort, a skirt portion formed integral with said barrel and extending longitudinally thereof and being disposed in spaced surrounding relationship to a portion of said boss, a plunger slidably positioned within said barrel, resilient piston means mounted on one end of said plunger and engaging the inner wall of said barrel, a hypodermic needle including a hub portion, said hub portion including an internal tapered bore complementary to the tapered outer surface of said boss, said hub being snugly received on said boss, the terminal end of said hub being disposed within said skirt portion, said skirt portion having a peripherally extending annular shoulder formed thereon and projecting inwardly therefrom, the end of said hub having a cooperating peripherally extending shoulder portion in engagement with the shoulder portion on said skirt portion for securely attaching the hub portion of the needle to the boss and skirt portion of the barrel of the syringe.

References Cited by the Examiner UNITED STATES PATENTS 2,972,991 2/1961 Burke l28218 3,021,942 2/1962 Hamilton 20643 3,073,307 1/1963 Stevens 128-221 3,199,748 8/1965 Bross 222-541 X ROBERT E. MORGAN, Primary Examiner.

D. L. TRULUCK, Assistant Examiner.

Claims (1)

1. 6. A DISPOSABLE STERILE MEDICAL AND SURGICAL DEVICE COMPRISING A HOLLOW BODY MEANS FORMED OF ORGANIC PLASTIC MATERIAL OF LOW MOLECULAR WEIGHT WHICH IS HARD FLOWING AND SETS UP QUICKLY IN A MOLD AND IS DIFFICULT TO BREAK, SAID BODY MEANS INCLUDING AN INTERMEDIATE FRANGIBLE PORTION FOR SEPARATING THE BODY MEANS INTO TWO SEPARATE PIECES, SO THAT THE BODY MEANS CANNOT BE EFFECTIVELY REUSED FOR ITS INTENDED PURPOSE, SAID FRANGIBLE PORTION INCLUDING A PRESTRESSED AREA HAVING A CONCENTRATION OF STRESSES THEREIN TO RENDER SAID AREA READILY BREAKABLE BY MANUAL EFFORT, AND ENCLOSURE MEANS DISPOSED IN TELESCOPING RELATIONSHIP WITH SAID BODY MEANS AND BEING ENGAGED THEREWITH TO DEFINE WITH THE BODY MEANS AN ENCLOSED SPACE.

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