Disclosure of Invention
The present invention is directed to solve at least some of the problems of the related art: the utility model provides an ultrasonic probe protective sheath, it can let medical personnel not bump the protective sheath with the protective sheath cover outside ultrasonic probe under the condition of touching the protective sheath lateral wall.
The present invention is directed to solve at least the second technical problem in the related art to some extent: the utility model provides a protective sheath erector, it can supply the ultrasonic probe protective sheath voluntarily to make medical personnel convenient operation.
To this end, an object of the present invention is to provide an ultrasound probe protection cover in view of the first technical problem, which is characterized by comprising:
the substrate is of an annular structure and is provided with a central channel for the ultrasonic probe to pass through;
a bottom film and a top film respectively sealing both ends of the central passage and configured to enable an end portion of the central passage to be opened under an acting force of the ultrasonic probe;
one end of the rubber sleeve is provided with an opening, the edge of the opening is rolled to form an annular rolling part, the part of the rubber sleeve, which is positioned outside the rolling part, is a flat part, and the rubber sleeve is arranged in the central channel;
the limiting piece is arranged in the central channel and is fixedly connected with the substrate;
when the ultrasonic probe penetrates through the central channel and pushes out the flat part of the rubber sleeve along the axial direction, the limiting sheet limits the furling part along the pushing-out direction Z of the ultrasonic probe. Because the existence of spacing piece, can support the roll-up portion that leans on the rubber sleeve at medical personnel's gripping substrate and this in-process spacing piece of passing ultrasonic probe along the axial cover to make the rubber sleeve can be expanded and the cover establish outside ultrasonic probe, medical personnel's hand only touches the lateral wall of substrate at this in-process, and contactless rubber sleeve.
According to an example of the present invention, the upper end surface of the stopper piece has a guide slope, and one side of the guide slope, which is far from the central passage, is higher than the other side of the guide slope, which is close to the central passage. Make medical personnel's gripping substrate and take off the in-process of rubber sleeve after ultrasonic examination accomplishes through setting up the inclined direction inclined plane that inclines inwards, the residue on the rubber sleeve lateral wall can assemble inwards under the water conservancy diversion effect on the inclined plane that leads, reduces even avoids the residue excessive.
The technical scheme has the following advantages or beneficial effects: firstly, medical care personnel only need to grasp the outer side wall of the substrate and align the central channel of the substrate with the top of the ultrasonic probe and then sleeve the ultrasonic probe, in the process, the flat part of the rubber sleeve covers the ultrasonic probe, the winding part of the rubber sleeve cannot be separated from the central channel of the substrate under the limiting action of the limiting sheet and can be continuously wound out along with the pulling of the flat part, and finally, the medical care personnel do not touch the rubber sleeve and can enable the whole rubber sleeve to be sleeved outside the ultrasonic probe; secondly, ultrasonic probe can directly burst basement membrane and apical membrane for medical personnel need not extra tear basement membrane and apical membrane, thereby brings the facility for medical personnel's use.
To this end, another objective of the present invention is to provide a cover mounter for the second technical problem, wherein: it includes barrel and a plurality of foretell ultrasonic probe protective sheath, storage piece chamber and working chamber have in the barrel, and each ultrasonic probe protective sheath is piled up in storage piece intracavity according to the preface along the thickness direction, be equipped with on the barrel and be used for ordering about each ultrasonic probe protective sheath of storage piece intracavity and send into the confession piece subassembly in the working chamber in proper order, the upper end of barrel has the up end with the working chamber intercommunication for supply the front end of ultrasonic probe to insert in the working chamber, the ultrasonic probe protective sheath in the working chamber is spacing in the working chamber along the direction of inserting of ultrasonic probe, when the front end of ultrasonic probe inserts in the working chamber the ultrasonic probe protective sheath overlaps outside ultrasonic probe.
According to an example of the invention, the outer side wall of the cylinder body is provided with a side opening which is communicated with the working cavity and extends to an upper port, and the width L of the side opening is matched with the size of the ultrasonic probe, so that the ultrasonic probe and the ultrasonic probe protective sleeve can move to the outside of the cylinder body along the horizontal direction through the side opening.
According to an example of the invention, the wafer supply assembly comprises a rotary table driven by a motor, the rotary table is positioned at the upper end of the wafer storage cavity, a clamping groove matched with the ultrasonic probe protective sleeve is formed in the rotary table, a spring assembly used for pushing the ultrasonic probe protective sleeve to move towards the position of the rotary table is arranged at the bottom of the wafer storage cavity, and the clamping groove drives the ultrasonic probe protective sleeves in the wafer storage cavity to sequentially move into the working cavity along with the rotation of the rotary table.
According to an example of the invention, the sheet supply assembly comprises a cover, the cover is detachably connected with the upper end of the cylinder and surrounds the upper end of the cylinder to form an accommodating cavity, an avoiding notch is formed in the position, corresponding to the upper port, of the cover, the rotary disc is in rotating fit with the accommodating cavity, the motor is arranged at the lower end of the cylinder, an output shaft of the motor is linked with the rotary disc through a transmission shaft, the transmission shaft is detachably connected with the rotary disc, and a shaft passage for the transmission shaft to pass through is formed in the cylinder.
According to an example of the invention, the device further comprises a connecting head and a mechanical arm, wherein two ends of the mechanical arm are respectively connected with the connecting head and the barrel; the connector is matched with an ultrasonic probe slot on the ultrasonic detection instrument, and a placing groove matched with the tail end of the ultrasonic probe with the electric wire is arranged on the connector.
The technical scheme has the following advantages or beneficial effects: a plurality of ultrasonic probe protective sheaths can be stored in storing up the piece chamber, and can be through supplying the piece subassembly with storing up the one by one of the ultrasonic probe protective sheath in the piece chamber deliver to the working chamber, medical personnel only need hold ultrasonic probe's tail end and make ultrasonic probe's front end insert the working chamber in can making ultrasonic probe's front end pass the ultrasonic probe protective sheath that is located the working chamber, make the synchronous cover of ultrasonic probe protective sheath establish outside ultrasonic probe's front end at this in-process, medical personnel need not both hands and grasp ultrasonic probe protective sheath and ultrasonic probe respectively and need manual alignment embolia from this, bring the facility for medical personnel's operation.
Additional aspects and advantages of the invention will be set forth in part in the description which follows and, in part, will be obvious from the description, or may be learned by practice of the invention.
Detailed Description
Reference will now be made in detail to embodiments of the present invention, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to the same or similar elements or elements having the same or similar functions throughout. The embodiments described below with reference to the drawings are illustrative and intended to be illustrative of the invention and are not to be construed as limiting the invention.
An ultrasound probe sheath and sheath installer according to an embodiment of the present invention will be described in detail below with reference to the accompanying drawings.
The ultrasonic probe protective sleeve is used for being sleeved on various slender ultrasonic probes in the existing ultrasonic examination process, including but not limited to being sleeved on a vaginal ultrasonic probe.
Basic embodiment of the ultrasonic probe protective sheath:
the invention provides an ultrasonic probe protective sleeve, which is characterized in that: the ultrasonic probe ejection device comprises a substrate 1, a rubber sleeve 5 and a limiting piece 6, wherein the substrate 1 is of an annular structure, a central channel 2 for an ultrasonic probe 10 to pass through is formed in the central position of the substrate 1, the rubber sleeve 5 is a soft sleeve with one end sealed and the other end provided with an opening, the rubber sleeve is of a strip-shaped thin-wall structure, the edge of the position of the opening of the rubber sleeve is turned inwards or outwards until the whole strip-shaped rubber sleeve 5 is wound into a flat structure, the flat rubber sleeve 5 after winding is provided with a flat part 5.2 located in the central position along the horizontal direction and a winding part 5.1 surrounding the flat part 5.2, the outer ring part of the winding 5.1 and the flat part 5.2 are of a continuous integrated structure, the flat rubber sleeve 5 after winding is arranged in the central channel 2 of the substrate 1, the limiting piece 6 is fixedly connected with the substrate 1, and when the ultrasonic probe 10 passes through the central channel 2 and pushes out the flat part 5.2 of the rubber sleeve 5 along the axial direction Z of the ultrasonic probe 10, the limiting piece 6 is wound along the axial direction of the limiting piece 5.1. Therefore, the flat part 5.2 can be ejected out of thecentral channel 2 along with theultrasonic probe 10, the furled part 5.1 which is furled in the whole process is restrained in thecentral channel 2 due to the restraint of the limitingsheet 6, the flat part 5.2 can pull the furled part 5.1 to be continuously unreeled, and finally the furled part 5.1 is continuously pulled out and sleeved outside theultrasonic probe 10.
The first embodiment of the ultrasonic probe protective sleeve is as follows:
based on the above basic embodiment, in order to make therubber sleeve 5 in a sterile state before use, it should be necessary to make thecentral channel 2 where therubber sleeve 5 is located in a sealed sterile state before use, and for this reason, the present embodiment provides an ultrasonic probe protection sleeve based on the above basic embodiment, which is characterized in that: thesubstrate 1, therubber sleeve 5 and the limitingsheet 6 are all located in the sealing bag. Medical personnel only need tear the sealed bag before using and graspsubstrate 1 can withsubstrate 1 intercommunication sets upspacing piece 6 onsubstrate 1 and therubber sleeve 5 that is locatedcentral channel 2 takes out, then overlaps onultrasonic probe 10, and this in-process medical personnel's hand only touchessubstrate 1 and does not have direct contact between 5 with the rubber sleeve.
The second embodiment of the ultrasonic probe protective sleeve:
although the first embodiment can solve the problem that therubber sleeve 5 can be maintained in a sterile state for a long time before use, a medical staff needs to tear the sealed bag during use, remove thesubstrate 1 from the sealed bag, and avoid touching therubber sleeve 5 during the process of removing thesubstrate 1, so that the solution of the sterile package of the first embodiment has the problem of inconvenient access, and therefore, the present invention provides an ultrasonic probe protection sleeve, as shown in fig. 1 to 6, which is characterized by comprising:
asubstrate 1, wherein thesubstrate 1 is of a ring-shaped structure and is provided with acentral channel 2 for anultrasonic probe 10 to pass through;
the sealing film is arranged on thesubstrate 1 and used for sealing two ends of thecentral channel 2, so that thecentral channel 2 and the sealing film surround to form a closed accommodating cavity;
therubber sleeve 5 is arranged in thecentral channel 2, one end of therubber sleeve 5 is provided with an opening, and the edge of the opening is turned over towards the other end of therubber sleeve 5 to enable therubber sleeve 5 to be in a flat structure, and therubber sleeve 5 in the flat structure is provided with an annular furling part 5.1 and a flat part 5.2 which is positioned in the furling part 5.1 along the horizontal direction;
the limitingpiece 6 is arranged in thecentral channel 2 and fixedly connected with thesubstrate 1, and when theultrasonic probe 10 penetrates through thecentral channel 2 and is axially ejected out of the flat part 5.2 of therubber sleeve 5, the limitingpiece 6 axially limits the furling part 5.1;
the moving direction of theultrasonic probe 10 penetrating through thecentral channel 2 is taken as an ejection direction Z, the sealing film comprises abottom film 4 and atop film 3 which are sequentially arranged along the ejection direction Z, and thebottom film 4 and thetop film 3 respectively seal two ends of thecentral channel 2; thebottom film 4 in this embodiment is a thin-walled film, and when theultrasonic probe 10 abuts against thebottom film 4 and applies an acting force on thebottom film 4, thebottom film 4 can be burst by theultrasonic probe 10, and thetop film 3 is connected with thesubstrate 1 in a tearable manner. Therefore, before the medical staff uses the ultrasonic probe, the medical staff only needs to tear off thetop film 3 on thesubstrate 1, then align the central position of the bottom film with theultrasonic probe 10, enable thebottom film 4 to be covered by the top film under the acting force of theultrasonic probe 10, and then abut against the flat part 5.2 to enable therubber sleeve 5 to be sleeved outside theultrasonic probe 10 in the process of moving relative to theultrasonic probe 10.
Thetop film 3 and thesubstrate 1 are connected to each other by means of, but not limited to, adhesive or heat sealing.
Preferably,basement membrane 4 is equipped with at least oneeasy tear line 8, as shown in fig. 2,easy tear line 8 is four, and foureasy tear lines 8 evenly arrange along circumference. The easily tornline 8 is a preset line on thebottom film 4, so that the thickness of thebottom film 4 on the line is smaller than the thickness of the part, outside the preset line, of thebottom film 4, thebottom film 4 can keep thecentral channel 2 sealed, and the bottom film can be broken along the easily tornline 8 when being subjected to the acting force of theultrasonic probe 10.
The third embodiment of the ultrasonic probe protective sleeve:
although the first embodiment described above can solve the problem that therubber sleeve 5 can be maintained in a sterile state for a long time before use, but the medical staff needs to tear the sealed bag during use, remove thesubstrate 1 from the sealed bag, and avoid touching therubber sleeve 5 during the process of removing thesubstrate 1, so that the problem of inconvenient access of the sterile packaging solution of the first embodiment can be seen, for this reason, the present invention provides an ultrasonic probe protection sleeve, as shown in fig. 3 to 7, which is characterized by comprising:
asubstrate 1, wherein thesubstrate 1 is in a ring structure and is provided with acentral channel 2 for anultrasonic probe 10 to pass through;
the sealing film is arranged on thesubstrate 1 and used for sealing two ends of thecentral channel 2, so that thecentral channel 2 and the sealing film surround to form a closed accommodating cavity;
therubber sleeve 5 is arranged in thecentral channel 2, one end of therubber sleeve 5 is provided with an opening, and the edge of the opening is turned over towards the other end of therubber sleeve 5, so that therubber sleeve 5 is in a flat structure, and therubber sleeve 5 in the flat structure is provided with an annular furling part 5.1 and a flat part 5.2 which is positioned in the furling part 5.1 along the horizontal direction;
the limitingpiece 6 is arranged in thecentral channel 2 and fixedly connected with thesubstrate 1, and when theultrasonic probe 10 penetrates through thecentral channel 2 and is axially ejected out of the flat part 5.2 of therubber sleeve 5, the limitingpiece 6 axially limits the furling part 5.1;
the moving direction of theultrasonic probe 10 penetrating through thecentral channel 2 is taken as an ejection direction Z, the sealing film comprises abottom film 4 and atop film 3 which are sequentially arranged along the ejection direction Z, and thebottom film 4 and thetop film 3 respectively seal two ends of thecentral channel 2;top membrane 3 andbasement membrane 4 in this embodiment are the thin film of thin wall,prop basement membrane 4 and exert effort in when onbasement membrane 4 atultrasonic probe 10basement membrane 4 can byultrasonic probe 10 bursting inwards, thenultrasonic probe 10 continues to offset along ejecting direction Z and the flat portion 5.2 ofrubber sleeve 5 and continues to drive flat portion 5.2 and the medial surface oftop membrane 3 and offsets, makes underultrasonic probe 10 along ejecting direction Z furthereffect top membrane 3 breaks outwards, and finallybasement membrane 4 andtop membrane 3 are backed up in order to makerubber sleeve 5 overlap in for the in-process ofultrasonic probe 10 motion outsideultrasonic probe 10.
Preferably, be equipped with at least one easily tearline 8 ontop film 3 and thebasement membrane 4 respectively, as shown in fig. 7, easily tearline 8 on thetop film 3 is four, and four easily tearline 8 evenly arrange along circumference. The easily tornline 8 is a preset line on thetop film 3, so that the thickness of thetop film 3 on the line is smaller than the thickness of the part, outside the preset line, of thetop film 3, thetop film 3 can keep thecentral channel 2 sealed, and the top film can be broken along the easily tornline 8 when being subjected to the acting force of theultrasonic probe 10. The easy-to-tear line 8 on thebottom film 4 and the easy-to-tear line 8 on thetop film 3 are of the same structure.
The fourth embodiment of the ultrasonic probe protective sleeve:
although the first embodiment described above can solve the problem that therubber sleeve 5 can be left in a sterile state for a long time before use, but a medical staff needs to tear the sealed bag during use, remove thesubstrate 1 from the sealed bag, and avoid touching therubber sleeve 5 during the process of removing thesubstrate 1, so that the solution of the sterile package of the first embodiment is inconvenient to take and use, and for this reason, the present invention provides an ultrasonic probe protection sleeve, as shown in the figure, which is characterized by comprising:
asubstrate 1, wherein thesubstrate 1 is in a ring structure and is provided with acentral channel 2 for anultrasonic probe 10 to pass through;
the sealing film is arranged on thesubstrate 1 and used for sealing two ends of thecentral channel 2, so that thecentral channel 2 and the sealing film surround to form a closed accommodating cavity;
therubber sleeve 5 is arranged in thecentral channel 2, one end of therubber sleeve 5 is provided with an opening, and the edge of the opening is turned over towards the other end of therubber sleeve 5 to enable therubber sleeve 5 to be in a flat structure, and therubber sleeve 5 in the flat structure is provided with an annular furling part 5.1 and a flat part 5.2 which is positioned in the furling part 5.1 along the horizontal direction;
the limitingpiece 6 is arranged in thecentral channel 2 and is fixedly connected with thesubstrate 1, and when theultrasonic probe 10 penetrates through thecentral channel 2 and axially ejects out of the flat part 5.2 of therubber sleeve 5, the limitingpiece 6 axially limits the furling part 5.1;
the moving direction of theultrasonic probe 10 penetrating through thecentral channel 2 is taken as an ejection direction Z, the sealing film comprises abottom film 4 and atop film 3 which are sequentially arranged along the ejection direction Z, and thebottom film 4 and thetop film 3 respectively seal two ends of thecentral channel 2; thebottom film 4 and thetop film 3 in this embodiment are each connected to thesubstrate 1 in a tearable manner. Therefore, before use, the medical staff only needs to grasp thesubstrate 1 and tear off thetop film 3 and thebottom film 4 on thesubstrate 1, then align thecentral channel 2 of thesubstrate 1 with theultrasonic probe 10, and abut against the flat part 5.2 in the process that theultrasonic probe 10 passes through thecentral channel 2, so that therubber sleeve 5 is sleeved outside theultrasonic probe 10 in the process of moving relative to theultrasonic probe 10.
Thetop film 3 and thesubstrate 1 and thebottom film 4 and thesubstrate 1 are connected to each other by means of, but not limited to, bonding or heat sealing.
Example v of the ultrasonic probe protective sheath:
based on the above-mentioned optimization of any embodiment, as shown in fig. 3, 5, and 6, with the moving direction of theultrasonic probe 10 passing through thecentral channel 2 as the ejection direction Z, that is, the ejection direction Z is upward in the vertical direction in fig. 3, the sealing film includes abottom film 4 and atop film 3 located above thebottom film 4, which are sequentially arranged along the ejection direction Z, and thebottom film 4 and thetop film 3 respectively seal the upper end and the lower end of thecentral channel 2; the limitingsheet 6 in the embodiment is of an annular structure, the outer edge of the limitingsheet 6 is fixedly connected with thesubstrate 1, and the limitingsheet 6 is located between the furling part 5.1 and thetop film 3.
Further, the inner edge of the limitingsheet 6 is bent towards the position of the furling part 5.1 to form an arc-shapedsection 7 matched with the outer contour of the furling part 5.1, that is, as shown in fig. 5, the inner edge of the limitingsheet 6 is bent downwards along the vertical direction to form an arc-shapedsection 7 matched with the outer contour of the furling part 5.1, and a distance h is left between the lower end of the arc-shapedsection 7 and thebottom film 4.
Preferably, the limitingsheet 6 and thesubstrate 1 are of an integral structure. Thesubstrate 1 and the limitingsheet 6 are made of plastic materials.
Sixth embodiment of the ultrasonic probe protective sheath:
medical personnel need get rid of old rubber sleeve 5 on ultrasonic probe 10 after the completion of vaginal ultrasound examination, because of the existence of substrate 1 this moment, consequently can make medical personnel grip substrate 1 and take off substrate 1 and rubber sleeve 5 from ultrasonic probe 10 and discard towards the top as shown in fig. 3, remaining liquid pollutant can be adhered to the surface of old rubber sleeve 5 this moment, medical personnel can make liquid pollutant assemble on substrate 1 and spill over medical personnel's hand or drip on the bottom surface of ultrasonic testing room in the in-process of pushing out substrate 1 upwards, based on this embodiment's further improvement lie in: the upper end surface of the limiting piece 6 is provided with a guide inclined surface 9, the outer edge of the guide inclined surface 9 is in transitional connection with the outer side surface of the substrate 1, the inner edge of the guide inclined surface 9 is in transitional connection with the side surface of the arc-shaped section 7, and one end of the guide inclined surface 9, which is far away from the central channel 2 along the radial direction, is higher than the other end of the guide inclined surface 2, namely the outer edge of the guide inclined surface 9 is higher than the inner edge of the guide inclined surface 9 along the vertical direction. At this moment, thesubstrate 1 drives the guideinclined plane 9 to move upwards relative to theultrasonic probe 10, and therubber sleeve 5 can be attached to the guideinclined plane 9, and the liquid pollutants on the outer surface of therubber sleeve 5 can flow along the position of thecentral channel 2 due to the inward inclination of the guideinclined plane 9, so that most of the liquid pollutants and even all of the liquid pollutants can be well kept in therubber sleeve 5. Of course, the inner and outer surfaces of therubber sleeve 5 are turned over in the process that therubber sleeve 5 is separated from theultrasonic probe 10, and the pollutants originally located on the outer side wall of therubber sleeve 5 can be left in therubber sleeve 5 along with the turning over of therubber sleeve 5.
Seventh embodiment of ultrasonic probe protective sheath:
in order to make the surface of therubber sleeve 5 wet and smooth, thecentral passage 2 is pre-filled with a liquid coupling agent. The couplant can play the role of lubricating therubber sleeve 5, and simultaneously can make the ultrasonic probe clearer in the using process. Preferably, the coupling agent is a medical sterilization coupling agent. The medical disinfection couplant is a couplant with a disinfection function, and is an existing commercially available product, so that the components of the medical disinfection couplant are not described in detail.
Eighth embodiment of the ultrasonic probe protective sheath:
as shown in fig. 5, since the width of thesubstrate 1 in the vertical direction is smaller in the present embodiment, the contact area with the outer side wall of thesubstrate 1 after the medical staff grips thesubstrate 1 is smaller, and the force is also transmitted to thesubstrate 1 during the process of applying the force to the sealing film and therubber sleeve 5 by theultrasonic probe 10 in the ejection direction Z, in order to make it easier for the medical staff to grip thesubstrate 1, the present embodiment is improved in that: the outer side wall of thesubstrate 1 is of a waist drum-shaped structure, wherein the diameter d1 of the middle position of the outer side wall is smaller than the diameter d2 of the two end positions of the outer side wall. Namely, thesubstrate 1 is of a circular ring structure, the middle position of thesubstrate 1 along the axial direction is radially inwards concave to form a waist drum-shaped structure with the diameter smaller than the diameters of the two end positions, and when each finger of a medical worker is gripped on the outer side wall of thesubstrate 1, the axial acting force can be more easily resisted when the finger is subjected to the axial acting force, so that thesubstrate 1 can be gripped more easily and conveniently.
The first embodiment of the protective sheath installer is as follows:
although the solution medical personnel who can be fine of each embodiment of above-mentioned ultrasonic probe protective sheath is avoiding the hand to touchrubber sleeve 5 at this in-process ofultrasonic probe 10 with ultrasonic probe protective sheath cover, nevertheless because the whole lamellar structure of ultrasonic probe protective sheath is unfavorable for medical personnel to hold. To this end, the present invention is intended to be further improved to achieve rapid installation of an ultrasound probe protective sheath on theultrasound probe 10. Therefore, based on the third embodiment of the ultrasonic probe protective sleeve and the fifth, sixth and seventh embodiments further improved by the third embodiment of the ultrasonic probe protective sleeve, the present invention provides a protective sleeve mounter, which is characterized in that: as shown in fig. 8 to 19, the ultrasonic diagnostic apparatus includes a cylinder 100 and a plurality of ultrasonic probe protection sleeves, the cylinder 100 has a sheet storage cavity 101 and a working cavity 102, each ultrasonic probe protection sleeve is sequentially stacked in the sheet storage cavity 101 along a thickness direction of the ultrasonic probe protection sleeve, the cylinder 100 is provided with a sheet supply assembly, the sheet supply assembly sequentially sends each ultrasonic probe protection sleeve in the sheet storage cavity 101 into the working cavity 102, that is, when there is no ultrasonic probe protection sleeve in the working cavity 102, the sheet supply assembly conveys one ultrasonic probe protection sleeve in the sheet storage cavity 101 into the working cavity 102, each ultrasonic probe protection sleeve in the sheet storage cavity 101 is sent into the working cavity 102 one by one along with the start and stop of the sheet supply assembly, the upper end of the cylinder 100 has an upper port 103 communicated with the working cavity 102 for inserting the front end of the ultrasonic probe 10 into the working cavity 102, the ultrasonic probe in the working cavity 102 is limited in the working cavity 102 along the insertion direction of the ultrasonic probe protection sleeve 10, when the front end of the ultrasonic probe 10 is inserted into the working cavity 102, the front end of the ultrasonic probe 10 passes through the inner end of the working cavity 102, and finally extends out of the ultrasonic probe protection sleeve 5.5.
Of course, in this embodiment, after the medical staff holds the tail end of theultrasound probe 10 and inserts the front end of theultrasound probe 10 into the workingchamber 102, the medical staff needs to take out theultrasound probe 10 and the ultrasound probe protection sleeve sleeved on theultrasound probe 10 from the workingchamber 102 for use in the ultrasound examination, at this time, if the medical staff exits from the upper port along the direction opposite to the insertion direction, the ultrasound probe protection sleeve in the workingchamber 102 should not be constrained by the workingchamber 102 along the direction opposite to the insertion direction of theultrasound probe 10.
The second embodiment of the protective sheath mounting device:
based on the first embodiment of the protective sheath installer described above, there is a risk that therubber sheath 5 is displaced relative to theultrasound probe 10 or even comes off theultrasound probe 10 during the process of withdrawing theultrasound probe 10 from the upper port, and therefore the improvement of this embodiment lies in: the outer side wall of thebarrel 100 is provided with aside opening 104 which is communicated with the workingcavity 102 and extends to anupper port 103, and the width L of theside opening 104 is matched with the size of theultrasonic probe 10, so that theultrasonic probe 10 and the protective sleeve of the ultrasonic probe can be translated to the outside of thebarrel 100 through theside opening 104. That is, after theultrasonic probe 10 is inserted into the workingchamber 102 from theupper port 103 in the axial direction, theultrasonic probe 10 can be translated to the right in the horizontal direction as shown in fig. 15 so as to be translated out of thebarrel 100 after passing through theside port 104. The advantage of doing so is that can makerubber sleeve 5 and the better laminating of the front end ofultrasonic probe 10 whenultrasonic probe 10 along the continuousejecting rubber sleeve 5 in the ultrasonic probe protective sheath of direction of insertion, then medical personnel exert horizontal direction's effort can withultrasonic probe 10 along with ultrasonic probe protective sheath slip out from workingchamber 102, this horizontal direction's effort can not causerubber sleeve 5 along axial slip, for this reason make can keep good laminating effect between thisrubber sleeve 5 and theultrasonic probe 10, and for ultrasonic examination, it is the important factor that influences ultrasonic examination effect to laminate closely and the zero clearance cavity between ultrasonic probe and therubber sleeve 5.
Third embodiment of the protective sheath installer:
based on the preferable example of the sheet supply assembly in each embodiment of the protective sheath mounter, as shown in fig. 15 to 17, the sheet supply assembly includes a turntable 200 driven by a motor 300, the motor 300 is fixedly mounted on the barrel 100, the turntable 200 is located at the upper end of the sheet storage cavity 101, a clamping groove 201 matched with the ultrasonic probe protective sheath is formed in the turntable 200, the clamping groove 201 alternately corresponds to the sheet storage cavity 101 and the working cavity 102 along with the rotation of the turntable 200, a spring assembly 900 for pushing the ultrasonic probe protective sheath to move towards the position of the turntable 200 is arranged at the bottom of the sheet storage cavity 101, so that under the thrust action of the spring assembly 900, each ultrasonic probe protective sheath stacked in the sheet storage cavity 101 has a tendency of moving upwards, a first ultrasonic probe protective sheath from top to bottom is located in the clamping groove 201, the first ultrasonic probe protective sheath is driven by the turntable to the working cavity 102 through the rotation of the turntable, and finally, each ultrasonic probe protective sheath in the sheet storage cavity 101 is continuously transferred into the working cavity 102 from top to bottom at intervals along with the continuous rotation of the turntable.
Preferably, as shown in fig. 17, the lockingslots 201 on therotating disc 200 may be one or more slots arranged along the circumference of the rotating disc. Specifically, the number of the clampinggrooves 201 is three, the three clampinggrooves 201 are arranged at intervals along the circumferential direction of theturntable 200, and any oneclamping groove 201 corresponds to thechip storage cavity 101 and the workingcavity 102 in sequence along with the circumferential rotation of theturntable 200.
Further, the number of thetablet storage cavities 101 is two or more, specifically, as shown in fig. 17, the number of thetablet storage cavities 101 is two, the twotablet storage cavities 101 and the workingcavity 102 are distributed at intervals along the circumferential direction of thebarrel 100, and the twotablet storage cavities 101 are respectively provided with respective ultrasonic probe protection sleeves andspring assemblies 900 for pushing the respective ultrasonic probe protection sleeves. Preferably, when the number of thesheet storage cavities 101 is two, the rotary table can adopt a mode of alternating forward rotation and reverse rotation to realize that the ultrasonic probe protective sleeves in the twosheet storage cavities 101 alternately move into the workingcavity 102, that is, the first ultrasonic probe protective sleeve at the topmost part in the firstsheet storage cavity 101 is driven into the workingcavity 102 when the rotary table 200 rotates forward, and the first ultrasonic probe protective sleeve at the topmost part in the secondsheet storage cavity 101 is driven into the workingcavity 102 when the rotary table 200 rotates reversely.
Preferably, as shown in fig. 11, thespring assembly 900 includes atop plate 901 and athrust spring 902, two ends of thethrust spring 902 respectively abut against thetop plate 901 and the bottom of thechip storage cavity 101, and thetop plate 901 abuts against the lowest ultrasonic probe protection sleeve, so that all the ultrasonic probe protection sleeves stacked in thechip storage cavity 101 are pushed to move upward under the action of thethrust spring 902.
Preferably, a first sensor for detecting whether an ultrasonic probe protective sleeve exists in the working cavity is arranged in the working cavity; and a counting sensor for detecting the number of the remaining ultrasonic probe protective sleeves in thewafer storage cavity 101 is arranged in thewafer storage cavity 101. The first sensor can be a laser sensor or a position sensor, the counting sensor can be a position sensor, the number of the remaining ultrasonic probe protective sleeves is calculated by detecting the position of the spring assembly, or the counting sensor can be an infrared sensor, and the number of the remaining ultrasonic probe protective sleeves is calculated by counting each ultrasonic probe protective sleeve after passing through the infrared sensor.
The fourth embodiment of the protective sheath installer:
based on the third embodiment of the protective sheath installer, when the ultrasonic probe 10 is inserted into the working cavity 102 from the upper port 102, there is contact between the ultrasonic probe 10 and the upper port 102, if there is contamination left in the continuous use process of the ultrasonic probe 10, the contamination on the ultrasonic probe 10 will contaminate the upper port 102, and for this reason, the improvement of this embodiment lies in: the sheet supply assembly comprises a cover 400, the cover 400 is detachably connected with the upper end of the cylinder body 100, the cover 400 and the upper end of the cylinder body 100 are encircled to form an accommodating cavity, the rotary table 200 is arranged in the accommodating cavity, the rotary table 200 is rotationally matched with the accommodating cavity around the axis of the rotary table 200, an avoiding notch 401 is arranged at the position, corresponding to the upper port 103, of the cover 400, the motor 300 is arranged at the lower end of the cylinder body 100, the output shaft of the motor 300 is linked with the rotary table 200 through a transmission shaft 500, the transmission shaft 500 is detachably connected with the rotary table 200, and a shaft passage 105 for the transmission shaft 500 to pass through is formed in the cylinder body 100. Through the design of themotor 300 and theturntable 200 in a split manner, thehousing 400 and theturntable 200 can be conveniently detached from the cylinder, so that thehousing 400 and theturntable 200 can be conveniently sterilized and cleaned regularly, and as shown in fig. 17 and 18, after the housing and theturntable 200 are detached, the upper port of thecylinder 100 can be well exposed, so that the sterilization and cleaning of the upper port are convenient. In the process, themotor 300 is located at the lower end position of thedrum 100 far away from the turntable, so that the motor and the circuit elements on the motor are not damaged in the disinfection process.
Fifth embodiment of the protective sheath installer:
based on each embodiment of above-mentioned protective sheath erector,barrel 100 of protective sheath erector can be held or shelved by medical personnel and be used for realizing establishingrubber sleeve 5 toultrasonic probe 10 cover on any mesa that can preventbarrel 100, but medical personnel need sit the place ahead atultrasonic detection instrument 800 in the ultrasonic detection room, andultrasonic detection instrument 800 is equipped with the sick bed that supplies the disease to lie on one side, therefore medical personnel can be more effective by the space of placing the protective sheath erector, for the protective sheath erector that makes this protective sheath erector do not occupy extra mesa space of the use this embodiment that makes medical personnel can be more convenient, for this improvement of this embodiment lies in: as shown in fig. 8 and 9, the present embodiment further includes aconnector 600 and arobot arm 700, wherein two ends of therobot arm 700 are respectively connected to theconnector 600 and thebarrel 100; theconnector 600 is matched with theultrasonic probe slot 801 on theultrasonic detection instrument 800, and theconnector 600 is provided with a holdinggroove 601 matched with the tail end of theultrasonic probe 10 with the electric wire.
Theultrasonic testing apparatus 800 is a generic name of an existing apparatus for ultrasonic testing, and includes a host part and one or more ultrasonic probes, the tail end of the ultrasonic probe is connected with the host through an electric wire, an operating console is provided on the host of theultrasonic testing apparatus 800, a plurality ofultrasonic probe slots 801 for placing the ultrasonic probes are provided on one side of the operating console, theultrasonic probe slots 801 on theultrasonic testing apparatus 800 are conventional structures in existing medical ultrasonic testing equipment, and therefore the structure of theultrasonic probe slots 801 is not described in detail.
Therest groove 601 in this embodiment is configured to match with the tail end of theultrasonic probe 10, so that theconnector 600 can be fixedly connected by using theultrasonic probe slot 801 on the existingultrasonic testing apparatus 800, and meanwhile, therest groove 601 additionally disposed on theconnector 600 can still be used for temporarily placing theultrasonic probe 10.
Themechanical arm 700 is preferably a mechanical arm for driving thecylinder 100 to hover at any position and direction.
Although embodiments of the present invention have been shown and described above, it will be understood that the above embodiments are exemplary and not to be construed as limiting the present invention, and that changes, modifications, substitutions and alterations can be made to the above embodiments by those of ordinary skill in the art within the scope of the present invention.
Various alterations and modifications will no doubt become apparent to those skilled in the art after having read the above description. Therefore, the appended claims should be construed to cover all such variations and modifications as fall within the true spirit and scope of the invention. Any and all equivalent ranges and contents within the scope of the claims should be considered to be within the intent and scope of the present invention.