CN216570084U - Clinical intrauterine hemostat for obstetrics and gynecology department - Google Patents
Clinical intrauterine hemostat for obstetrics and gynecology department Download PDFInfo
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- CN216570084U CN216570084U CN202123004425.4U CN202123004425U CN216570084U CN 216570084 U CN216570084 U CN 216570084U CN 202123004425 U CN202123004425 U CN 202123004425U CN 216570084 U CN216570084 U CN 216570084U
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- obstetrics
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- 239000002874 hemostatic agent Substances 0.000 title claims abstract description 15
- 238000007789 sealing Methods 0.000 claims description 18
- 239000007788 liquid Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 12
- 239000008280 blood Substances 0.000 abstract description 28
- 210000004369 blood Anatomy 0.000 abstract description 28
- 210000005077 saccule Anatomy 0.000 abstract description 20
- 230000023597 hemostasis Effects 0.000 abstract description 15
- 230000002439 hemostatic effect Effects 0.000 abstract description 5
- 239000003814 drug Substances 0.000 description 18
- 230000000903 blocking effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 208000018525 Postpartum Hemorrhage Diseases 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 208000006083 Hypokinesia Diseases 0.000 description 1
- 208000034693 Laceration Diseases 0.000 description 1
- 208000036029 Uterine contractions during pregnancy Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 210000002826 placenta Anatomy 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
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Abstract
The utility model discloses a clinical intrauterine hemostat for obstetrics and gynecology department, which comprises an outer saccule, wherein the inner side of the outer saccule is fixedly connected with an inner saccule, the inner side of the outer saccule is provided with a first catheter, the bottom end of the first catheter is communicated with a collecting bag, the inner side of the first catheter is fixedly connected with a third catheter, the other end of the third catheter is communicated with a first needle tube, the inner side of one end of the first catheter is communicated with a second catheter, compared with the prior art, when the inner saccule and the outer saccule are inflated in an intrauterine cavity for hemostasis, the position of the first catheter in the intrauterine cavity is adjusted to enable the first catheter to be in contact with the blood in the intrauterine cavity, when the blood in the intrauterine cavity is less, the blood can be sucked out through the third needle tube, when the blood in the intrauterine cavity is more, the blood can be automatically remained to the inner side of the collecting bag through the first catheter, and further the hemostatic effect can be judged through the amount of the blood flowing out, meanwhile, the skin on the inner side of the uterine cavity can be placed through the hemispheroid to block the inlet of the first conduit.
Description
Technical Field
The utility model relates to the field of hemostats, in particular to a clinical intrauterine hemostat for obstetrics and gynecology department.
Background
The pathogenesis of postpartum hemorrhage is uterine contraction hypodynamia, flaccid birth canal laceration, placenta factor and blood coagulation dysfunction in sequence, the four causes can exist in a combined way or be cause and effect mutually, and the postpartum hemorrhage is treated by rapid hemostasis and early intervention treatment which is very important.
At present when stanching the palace intracavity, generally use the sacculus hemostasis by compression, when using the sacculus hemostasis by compression, the partial blood of hemostasis in-process exhaust can not flow, and then can not judge hemostatic effect according to the flow of blood, influence medical staff's work, the body fluid of palace intracavity also can not in time be discharged simultaneously, and can not carry out the medicine loading when stanching through the sacculus hemostasis by compression, also do not benefit to medical staff's work, for this reason, we provide a clinical palace intracavity haemostat of gynaecology and obstetrics.
SUMMERY OF THE UTILITY MODEL
The utility model mainly aims to provide a clinical intrauterine hemostat for obstetrics and gynecology department, which can effectively solve the problems in the background technology.
In order to achieve the purpose, the utility model adopts the technical scheme that:
the utility model provides a clinical palace intracavity haemostat of gynaecology and obstetrics, includes outer sacculus, sacculus in the inboard fixedly connected with of outer sacculus, the inboard of outer sacculus is provided with first pipe, the bottom intercommunication of first pipe has the collection bag, the inboard fixedly connected with third pipe of first pipe, the other end intercommunication of third pipe has first needle tubing, the inboard intercommunication of one end of first pipe has the second pipe, the other end intercommunication of second pipe has third needle tubing.
Furthermore, through holes are formed in the inner side of the periphery of the outer balloon, the periphery of the inner balloon is fixedly connected with blocking blocks, and the blocking blocks are clamped with the through holes.
Furthermore, the outer sides of the first conduit and the second conduit are both communicated with a second stop valve, and the outer side of the third conduit is communicated with a third stop valve.
Further, the top end of the outer balloon and the inner side of the bottom end of the outer balloon are fixedly connected with fixing rings, the inner sides of the fixing rings are rotatably connected with sealing rings, the sealing rings are fixedly connected with a first conduit, and the first conduit is rotatably connected with the fixing rings through the sealing rings.
Furthermore, a liquid inlet is formed in one end of the first conduit, a hemisphere is arranged around the liquid inlet and fixedly connected with the first conduit.
Furthermore, one end of the outer balloon is communicated with a third catheter, the other end of the third catheter is communicated with a second needle tube, and the outer side of the third catheter is communicated with a first stop valve.
Further, one end of the third catheter extends out of one end of the first catheter and is positioned on the inner side of the inner balloon.
The utility model has the following beneficial effects:
compared with the prior art, through the outer sacculus that is equipped with, interior sacculus, first pipe, collect the bag, the second pipe, the third pipe, gu fixed ring, the sealing ring, hemisphere and third needle tubing, interior sacculus and outer sacculus are when the hemostasis of inflating in palace chamber, through the position of adjusting first pipe in palace chamber, make first pipe and the interior blood contact of palace chamber, when blood is less in palace chamber, can be through the suction of blood of third needle tubing, when blood is more in palace chamber, blood can stay the inboard of collecting the bag through first pipe is automatic, and then judge hemostatic effect through the volume that blood flows out, can place the inboard skin of palace chamber through the hemisphere simultaneously and plug up the entry of first pipe.
Compared with the prior art, through the inner saccule, the block, the first stop valve, the third conduit and the second needle tube which are arranged, when the medicine is required to be sprayed in the uterine cavity, the medicine can be sprayed into the uterine cavity through the third conduit and the through hole, and the inner saccule is matched with the outer saccule to realize the effect of hemostasis when hemostasis is performed.
Drawings
In order to more clearly illustrate the technical solution of the present invention, the drawings needed to be used in the technical description of the present invention will be briefly introduced below, and it is apparent that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained according to the drawings without inventive labor.
FIG. 1 is a schematic overall structure diagram of a clinical intrauterine hemostat of obstetrics and gynecology department of the utility model;
FIG. 2 is a schematic view of a mounting structure of a first syringe according to the present invention;
FIG. 3 is a schematic view of an enlarged internal mounting arrangement for an inner balloon in accordance with the present invention;
FIG. 4 is a schematic view of the inner balloon of the present invention shown in a configuration when not in use;
fig. 5 is a schematic view of the installation structure of the hemisphere of the present invention.
In the figure: 1. an outer balloon; 2. a first conduit; 3. a collection bag; 4. a second conduit; 5. a first shut-off valve; 6. a third conduit; 7. a fixing ring; 8. a seal ring; 9. a hemisphere; 10. an inner balloon; 11. blocking; 12. a first needle tube; 13. a third conduit; 14. a second needle tube; 15. a through hole; 16. a second stop valve; 17. a third stop valve; 18. a third needle tube; 19. and (4) a liquid inlet.
Detailed Description
The present invention will be further described with reference to the following detailed description, wherein the drawings are for illustrative purposes only and are not intended to be limiting, wherein certain elements may be omitted, enlarged or reduced in size, and are not intended to represent the actual dimensions of the product, so as to better illustrate the detailed description of the utility model.
Example 1
As shown in fig. 1-5, a clinical intrauterine hemostat for obstetrics and gynecology department comprises an outer balloon 1, an inner balloon 10 fixedly connected to the inner side of the outer balloon 1, a first catheter 2 arranged on the inner side of the outer balloon 1, a collecting bag 3 communicated with the bottom end of the first catheter 2, a third catheter 13 fixedly connected to the inner side of the first catheter 2, a first needle tube 12 communicated with the other end of the third catheter 13, a second catheter 4 communicated with the inner side of one end of the first catheter 2, and a third needle tube 18 communicated with the other end of the second catheter 4.
By adopting the technical scheme: through-hole 15 has been seted up to outer sacculus 1 inboard all around, and inner sacculus 10 fixedly connected with sprue 11 all around, and the mutual block of sprue 11 and through-hole 15 is convenient for realize the sealed of outer sacculus 1.
By adopting the technical scheme: the outer sides of the first conduit 2 and the second conduit 4 are both communicated with a second stop valve 16, and the outer side of the third conduit 13 is communicated with a third stop valve 17, so that the first conduit 2 and the second conduit 4 can be conveniently sealed.
By adopting the technical scheme: the top of outer sacculus 1 and the solid fixed ring 7 of the inboard equal fixedly connected with in bottom, the inboard rotation of solid fixed ring 7 is connected with sealing ring 8, sealing ring 8 and 2 fixed connection of first pipe, first pipe 2 is made by nonrust steel pipe, the rotation of the first pipe 2 of being convenient for, and first pipe 2 passes through sealing ring 8 and solid fixed ring 7 and rotates and be connected, when guaranteeing that first pipe 2 rotates, blood can not be just like the inboard of outer sacculus 1.
By adopting the technical scheme: a liquid inlet 19 is formed in one end of the first conduit 2, a hemisphere 9 is arranged on the periphery of the liquid inlet 19, the hemisphere 9 is fixedly connected with the first conduit 2, and the skin on the inner side of the uterine cavity can be placed through the hemisphere 9 to plug the inlet of the first conduit 2.
By adopting the technical scheme: one end of the third catheter 13 extends out of the first catheter 2 and is positioned on the inner side of the inner balloon 10, so that the inner balloon 10 can be inflated conveniently.
The working process is as follows: when the utility model is used, firstly, the uninflated outer saccule 1 and the inner saccule 10 are put into the uterine cavity, then the third stop valve 17 is opened, and then the inner side of the inner balloon 10 is inflated through the first needle tube 12 and the third catheter 13, so that the inner balloon 10 gradually props up the outer balloon 1 to realize the hemostasis in the uterine cavity, meanwhile, the worker rotates the first conduit 2, and the first conduit 2 also drives the sealing ring 8 to rotate at the inner side of the fixing ring 7, so that the liquid inlet 19 of the first conduit 2 is positioned below the uterine cavity, when the blood in the uterine cavity is small and can not be discharged by the staff, the staff leads the third needle tube 18 to draw the blood out of the uterine cavity through the second catheter 4 and the first catheter 2, and then judge hemostatic effect through the blood of taking out, when blood can oneself be discharged, blood can flow into collection bag 3 along first pipe 2, and then can judge hemostatic effect through the blood volume of collecting bag 3 inboard.
Example 2
As shown in fig. 1-4, a clinical intrauterine hemostat for obstetrics and gynecology department comprises an outer saccule 1, an inner saccule 10 fixedly connected with the inner side of the outer saccule 1, a first conduit 2 arranged at the inner side of the outer saccule 1, a collecting bag 3 communicated with the bottom end of the first conduit 2, a third conduit 13 fixedly connected with the inner side of the first conduit 2, a first needle tube 12 communicated with the other end of the third conduit 13, a second conduit 4 communicated with the inner side of one end of the first conduit 2, and a third needle tube 18 communicated with the other end of the second conduit 4.
By adopting the technical scheme: through-hole 15 has been seted up to the inboard all around of outer sacculus 1, fixedly connected with sprue 11 all around of interior sacculus 10, and the mutual block of sprue 11 and through-hole 15 is convenient for realize sealed to outer sacculus 1.
By adopting the technical scheme: the outer sides of the first conduit 2 and the second conduit 4 are both communicated with a second stop valve 16, and the outer side of the third conduit 13 is communicated with a third stop valve 17, so that the first conduit 2 and the second conduit 4 can be conveniently sealed.
By adopting the technical scheme: the top of outer sacculus 1 and the solid fixed ring 7 of the inboard equal fixedly connected with in bottom, the inboard rotation of solid fixed ring 7 is connected with sealing ring 8, sealing ring 8 and 2 fixed connection of first pipe, first pipe 2 is made by nonrust steel pipe, the rotation of the first pipe 2 of being convenient for, and first pipe 2 passes through sealing ring 8 and solid fixed ring 7 and rotates and be connected, when guaranteeing that first pipe 2 rotates, blood can not be just like the inboard of outer sacculus 1.
By adopting the technical scheme: a liquid inlet 19 is formed in one end of the first conduit 2, a hemisphere 9 is arranged on the periphery of the liquid inlet 19, the hemisphere 9 is fixedly connected with the first conduit 2, and the skin on the inner side of the uterine cavity can be placed through the hemisphere 9 to block the inlet of the first conduit 2.
By adopting the technical scheme: one end of the outer balloon 1 is communicated with a third catheter 6, the other end of the third catheter 6 is communicated with a second needle tube 14, and the outer side of the third catheter 6 is communicated with a first stop valve 5, so that medicine can be conveniently input to the inner side of the outer balloon 1.
By adopting the technical scheme: one end of the third catheter 13 extends out of the first catheter 2 and is positioned on the inner side of the inner balloon 10, so that the inner balloon 10 can be inflated conveniently.
The working process comprises the following steps: when the medicine spraying device is used, when medicine needs to be sprayed into a uterine cavity, the medicine is firstly put into the inner side of the second needle tube 14, then the first stop valve 5 is opened, then the medicine is input into the inner side of the third catheter 6 through the second needle tube 14, gas inside the third catheter 6 is discharged through the first stop valve 5, then the first stop valve 5 is closed, part of the gas inside the inner balloon 10 is pumped out through the first needle tube 12, the blocking block 11 is separated from the through hole 15, then the medicine is continuously introduced into the inner side of the third catheter 6 through the second needle tube 14, the medicine enters the uterine cavity through the third catheter 6 and the through hole 15 inside the outer balloon 1, and after medicine feeding is completed, the inner side of the inner balloon 10 is continuously inflated, and hemostasis is carried out again.
Example 3
As shown in fig. 1-5, a clinical intrauterine hemostat for obstetrics and gynecology department comprises an outer balloon 1, an inner balloon 10 fixedly connected to the inner side of the outer balloon 1, a first catheter 2 arranged on the inner side of the outer balloon 1, a collecting bag 3 communicated with the bottom end of the first catheter 2, a third catheter 13 fixedly connected to the inner side of the first catheter 2, a first needle tube 12 communicated with the other end of the third catheter 13, a second catheter 4 communicated with the inner side of one end of the first catheter 2, and a third needle tube 18 communicated with the other end of the second catheter 4.
By adopting the technical scheme: through-hole 15 has been seted up to outer sacculus 1 inboard all around, and inner sacculus 10 fixedly connected with sprue 11 all around, and the mutual block of sprue 11 and through-hole 15 is convenient for realize the sealed of outer sacculus 1.
By adopting the technical scheme: the outer sides of the first conduit 2 and the second conduit 4 are both communicated with a second stop valve 16, and the outer side of the third conduit 13 is communicated with a third stop valve 17, so that the first conduit 2 and the second conduit 4 can be conveniently sealed.
By adopting the technical scheme: the top of outer sacculus 1 and the solid fixed ring 7 of the inboard equal fixedly connected with in bottom, the inboard rotation of solid fixed ring 7 is connected with sealing ring 8, sealing ring 8 and 2 fixed connection of first pipe, first pipe 2 is made by nonrust steel pipe, the rotation of the first pipe 2 of being convenient for, and first pipe 2 passes through sealing ring 8 and solid fixed ring 7 and rotates and be connected, when guaranteeing that first pipe 2 rotates, blood can not be just like the inboard of outer sacculus 1.
By adopting the technical scheme: a liquid inlet 19 is formed in one end of the first conduit 2, a hemisphere 9 is arranged on the periphery of the liquid inlet 19, the hemisphere 9 is fixedly connected with the first conduit 2, and the skin on the inner side of the uterine cavity can be placed through the hemisphere 9 to block the inlet of the first conduit 2.
By adopting the technical scheme: one end of the outer balloon 1 is communicated with a third catheter 6, the other end of the third catheter 6 is communicated with a second needle tube 14, and the outer side of the third catheter 6 is communicated with a first stop valve 5, so that medicine can be conveniently input to the inner side of the outer balloon 1.
By adopting the technical scheme: one end of the third catheter 13 extends out of the first catheter 2 and is positioned on the inner side of the inner balloon 10, so that the inner balloon 10 can be inflated conveniently.
The working process comprises the following steps: when the utility model is used, firstly, the uninflated outer saccule 1 and the inner saccule 10 are placed into the uterine cavity, then the third stop valve 17 is opened, then the first needle tube 12 is used for inflating towards the inner side of the inner saccule 10 through the third catheter 13, so that the inner saccule 10 gradually supports the outer saccule 1 to realize the hemostasis in the uterine cavity, meanwhile, a worker rotates the first catheter 2, the first catheter 2 can also drive the sealing ring 8 to rotate at the inner side of the fixing ring 7, so that the liquid inlet 19 of the first catheter 2 is positioned below the uterine cavity, when the blood amount in the uterine cavity is small and can not be discharged by himself, the worker can drive the third needle tube 18 to draw the blood out of the uterine cavity through the second catheter 4 and the first catheter 2, and then the hemostasis effect can be judged through the drawn blood, when the blood can be discharged by himself, the blood can flow into the collection bag 3 along the first catheter 2, and then the hemostasis effect can be judged through the blood amount in the inner side of the collection bag 3, when medicine needs to be sprayed into the uterine cavity, the medicine is firstly put into the inner side of the second needle tube 14, then the first stop valve 5 is opened, then the medicine is input into the inner side of the third catheter 6 through the second needle tube 14, gas inside the third catheter 6 is discharged through the first stop valve 5, then the first stop valve 5 is closed, then the gas inside the inner balloon 10 is pumped out through the first needle tube 12, the blocking block 11 is separated from the through hole 15, then the medicine is continuously fed into the inner side of the third catheter 6 through the second needle tube 14, so that the medicine enters the uterine cavity through the third catheter 6 and the through hole 15 inside the outer balloon 1, and after medicine feeding is completed, the inner side of the inner balloon 10 is continuously inflated, and hemostasis is performed again.
The foregoing shows and describes the general principles and broad features of the present invention and advantages thereof. It will be understood by those skilled in the art that the present invention is not limited to the embodiments described above, which are described in the specification and illustrated only to illustrate the principle of the present invention, but that various changes and modifications may be made therein without departing from the spirit and scope of the present invention, which fall within the scope of the utility model as claimed. The scope of the utility model is defined by the appended claims and equivalents thereof.
Claims (7)
1. The utility model provides a clinical palace intracavity haemostat of gynaecology and obstetrics, includes outer sacculus (1), its characterized in that: sacculus (10) in the inboard fixedly connected with of outer sacculus (1), the inboard of outer sacculus (1) is provided with first pipe (2), the bottom intercommunication of first pipe (2) has collection bag (3), the inboard fixedly connected with third pipe (13) of first pipe (2), the other end intercommunication of third pipe (13) has first needle tubing (12), the inboard intercommunication of one end of first pipe (2) has second pipe (4), the other end intercommunication of second pipe (4) has third needle tubing (18).
2. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: through-holes (15) have been seted up to the inboard all around of outer sacculus (1), fixedly connected with sprue (11) all around of interior sacculus (10), and sprue (11) and through-hole (15) block each other.
3. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: and the outer sides of the first conduit (2) and the second conduit (4) are both communicated with a second stop valve (16), and the outer side of the third conduit (13) is communicated with a third stop valve (17).
4. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: the top and the inboard solid fixed ring of all fixedly connected with (7) in bottom of outer sacculus (1), the inboard rotation of solid fixed ring (7) is connected with sealing ring (8), sealing ring (8) and first pipe (2) fixed connection, and first pipe (2) rotate with solid fixed ring (7) through sealing ring (8) and are connected.
5. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: a liquid inlet (19) is formed in one end of the first conduit (2), a hemisphere (9) is arranged on the periphery of the liquid inlet (19), and the hemisphere (9) is fixedly connected with the first conduit (2).
6. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: one end of the outer balloon (1) is communicated with a third conduit (13), the other end of the third conduit (13) is communicated with a second needle tube (14), and the outer side of the third conduit (13) is communicated with a first stop valve (5).
7. The intrauterine hemostat for obstetrics and gynecology clinic according to claim 1, wherein: one end of the third catheter (13) extends out of the first catheter (2) and is positioned on the inner side of the inner balloon (10).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202123004425.4U CN216570084U (en) | 2021-12-02 | 2021-12-02 | Clinical intrauterine hemostat for obstetrics and gynecology department |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202123004425.4U CN216570084U (en) | 2021-12-02 | 2021-12-02 | Clinical intrauterine hemostat for obstetrics and gynecology department |
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| Publication Number | Publication Date |
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| CN216570084U true CN216570084U (en) | 2022-05-24 |
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| Application Number | Title | Priority Date | Filing Date |
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| CN202123004425.4U Expired - Fee Related CN216570084U (en) | 2021-12-02 | 2021-12-02 | Clinical intrauterine hemostat for obstetrics and gynecology department |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115363675A (en) * | 2022-09-21 | 2022-11-22 | 刘燕 | A device that stanchs fast for metrorrhagia |
-
2021
- 2021-12-02 CN CN202123004425.4U patent/CN216570084U/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115363675A (en) * | 2022-09-21 | 2022-11-22 | 刘燕 | A device that stanchs fast for metrorrhagia |
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Granted publication date: 20220524 |