19 results about "Cervical canal" patented technology

A method of uterine hemostasis involves inserting a suction line of a postpartum hemorrhage mitigation device through a cesarian incision into the uterine cavity, guiding the suction line through the cervix and into the vagina, positioning an anchoring mechanism of the device adjacent the internal cervical OS of the uterine cavity, closing the cesarian incision to enclose the suction line within the uterine cavity, and connecting the suction line to a negative pressure source that introduces negative pressure to the uterine cavity via the suction line, thereby causing contraction of the uterus and evacuation of fluid from the uterus via the suction line extension. Upon completion of a treatment period, the negative pressure source is disconnected, and the suction line and anchoring mechanism are extracted from the uterus through the cervical canal and the vagina.

The invention discloses a gynecological nursing cervix uteri medicine applying device, belongs to the technical field of cervix uteri medicine applying, and aims to solve the problems that liquid medicine is discharged in a fixed-point spraying mode, can only act on a local area of a cervix uteri external opening in a concentrated mode, is difficult to uniformly cover the inner wall of a cervix uteri canal and is prone to being too high in local liquid medicine concentration. A connecting rod is rotatably connected to one end of the guide pipe, a threaded cylinder is fixedly mounted on the surface of the connecting rod, a one-way liquid storage cylinder is fixedly mounted at one end of the connecting rod, the one-way liquid storage cylinder is slidably connected with the interior of one end of the extending pipe, and a plurality of liquid spraying pieces are arranged on the surface of the one-way liquid storage cylinder. The one-way liquid storage barrel and the liquid spraying piece are driven to rotate synchronously and are matched with the piston rod to extrude out liquid, so that the liquid medicine completely covers the inner wall of the cervical canal and the whole circumference of the cervix uteri in a centrifugal mode, and the problems that traditional medicine feeding is uneven and the local liquid medicine concentration is too high are solved.

The application discloses a reproductive secretion sampling device and relates to the technical field of medical diagnosis sampling, and aims to solve the technical problem that cervical canal secretion sampling is easily affected by external environment. The application solves the pain point of traditional sampling through multidimensional design, guarantees sample quality and operation convenience, and greatly reduces the pollution risk through the whole sealing structure, from the extension of the sampling cotton swab, sampling to falling into the container, and automatic sealing of the sealing cover. The fixed part and the loose card structure realize convenient installation and stable fixation of the sampling cotton swab, and prevent the sampling cotton swab from falling off during sampling. The multi-angle sealing design of the sealing cover prevents the storage liquid from pouring when the sealing cover is inclined. The adjustable pressure receiving strip is suitable for sampling containers with different diameters, and the universality is enhanced. The moisture-absorbing inner layer of the port cover and the elastic return structure reduce the interference of vaginal secretion, improve the sample purity, and overall meet the sterile, stable and adaptive clinical sampling requirements, and guarantee the accuracy of the detection result.

The multi-channel device comprises a multi-channel hysteroscope device body, a main body is arranged on the multi-channel hysteroscope device body, a soft supporting sleeve is arranged on the left side of the main body in a matched mode, an inner cavity is formed in the main body, and an anti-falling hoop is arranged on the inner side, close to a side port, of the inner cavity in the main body. The outer ring of the main body wraps the air bag and is adhered to the outer wall of the main body, an inner cavity of the main body is filled with gelatin and is formed by integral injection molding, an air inlet hole is formed in the outer side of the main body, the air inlet hole and the main body are of an integral structure, and a silicone tube is connected to the outside of a port of the air inlet hole. After the air bag is expanded, the main body is firmly clamped into the vagina and is not prone to falling off, the air bag can be easily taken out after water in the air bag is discharged after an operation is completed, and gelatin in the main body has good sealing performance.

This utility model discloses a postpartum hemorrhage blood measurement kit, including a cervical canal connecting ring with a front end and hollow side walls. A vaginal dilator with a similarly hollow side walls is connected to the rear end of the cervical canal connecting ring. A support plate is mounted on the rear end of the vaginal dilator via a sealing base plate and a connecting piece. The support plate has a collection hole, an observation hole, and a processing hole. A blood collection head is installed in the collection hole, and its rear end is connected to a blood measurement container via a collection tube and a connecting hose. An observation operation tube is inserted into the observation hole, and a high-definition medical camera is mounted at its front end, connected to a medical monitor. A sealing plug is installed in the processing hole. The advantages of this utility model are: ease of use, real-time observation capability, accurate blood measurement, and the ability to provide immediate and rapid treatment for adverse conditions in postpartum women or patients, effectively preventing life-threatening situations.

This invention discloses a cervical thermocoagulation device, belonging to the field of surgical diagnostic and therapeutic instrument technology. It includes a basic component comprising an operating rod, which consists of a handle and a shaft tube, and a treatment head connected to one end of the shaft tube. An expansion component includes an elastic mesh tube, a fixing ring, and a permanent magnet ring fixedly connected to both ends of the elastic mesh tube. In its natural state, the elastic mesh tube is shaped like a date pit with a radial bulge in the middle. The fixing ring is fixedly connected to the end of the shaft tube near the treatment head, and the permanent magnet ring is sleeved on the shaft tube and located on the side of the fixing ring opposite to the treatment head. This invention uses the radial expansion of the elastic mesh tube to form a hollow channel and open the cervical wall, allowing for full exposure of the lesion and a continuously clear surgical field. Relying on the superelastic properties of the elastic mesh tube, the treatment head can be flexibly adjusted within a safe range, while avoiding the safety hazard of burns to the cervical canal or normal uterine tissue due to accidental insertion.

The utility model discloses a cervical contractor which comprises an elastic constriction piece which is suitable for being hooped on a cervical canal so as to seal a cervical opening. The elastic contraction piece comprises a lantern ring part and a holding structure, and the lantern ring part is suitable for being arranged on the cervical canal in a sleeving mode; the enclasping structure is arranged in the circumferential direction of the lantern ring part in a surrounding mode and can tighten the cervical canal. According to the cervical contractor provided by the embodiment of the utility model, the cervical contractor can be flexibly hooped on a cervical canal to realize effective sealing of a cervical orifice, so that premature delivery of a fetus is prevented. Compared with a traditional method, the operation process is greatly simplified through the design, complex suture and suture removing processes are not needed, and the infection risk and the complication occurrence rate are remarkably reduced. Meanwhile, due to the elastic characteristic, appropriate adjustment can be conducted according to natural changes of the cervix uteri, the comfort level of the pregnant woman is improved, and discomfort is reduced. In addition, by means of the non-invasive design, damage to cervical tissue is greatly reduced, and psychological burden is relieved.

This utility model relates to the field of medical device technology and discloses a cervical stent structure for use with a Gynee IUD, which is installed in the uterine cavity. The cervical stent structure includes a connecting rod and an elastic support assembly: the first end of the connecting rod along its length is used for fixed connection to the Gynee IUD; the elastic support assembly is disposed on the outer circumferential surface of the connecting rod and is used for insertion into the cervical canal for support. The elastic support assembly has a first state of compression and radial contraction, and a second state of expansion and unfolding. The size of the elastic support assembly in the first state is smaller than the size of the cervical canal, and the size of the elastic support assembly in the second state is larger than the size of the cervical canal. This utility model can effectively prevent the cervical canal walls from approaching each other radially along the connecting rod and recurring adhesions.

The invention discloses a uterine cavity perfusion liquid medicine retaining and flushing device, and relates to the technical field of lavage, the uterine cavity perfusion liquid medicine retaining and flushing device comprises a perfusion tube, a moving part, a distance adjusting part and a bag part, under the adjustment of the distance adjusting part and the control of the moving part, the bag part is inflated under the two conditions that the vagina is close to the cervical opening and the cervical canal position, and liquid medicine is prevented from overflowing; and the retention time is controlled by medical personnel according to the condition of the patient.

The invention discloses a uterus lifting device which comprises a uterus lifting mechanism, a clamping mechanism and a telescopic mechanism, the clamping mechanism is arranged on the uterus lifting mechanism in a penetrating mode, and the telescopic mechanism is connected with the clamping mechanism in a matched mode; when the uterine manipulator is used, the uterine lifting mechanism is arranged at the position of a cervical canal of a patient, and the telescopic mechanism drives the clamping mechanism to fix the cervical canal. The clamping mechanism is arranged in the uterus lifting mechanism, and the telescopic mechanism is connected with the clamping mechanism in a matched mode, so that the telescopic mechanism can drive the clamping mechanism to clamp the cervical canal; the cervical device can be matched with cervical canals with different diameters, the cervical device can be fixed and is not prone to slipping in an operation, the force for dragging the uterus outwards can be provided, and the requirement for exposure of the operation is better met; the device is simple in structure, high in practicability and good in experience feeling of surgeons.

An insert (1100, 1300, 1400, 1500) for an intrauterine system (1102, 1336, 1402, 1502) is disclosed, comprising: a handle body (1104, 1306, 1416, 1504), a measuring tube (1110, 1328, 1406, 1510), a plunger (1132, 1202, 1362, 1450, 1532), a flange (1122, 1404, 1522), a finger retainer (1124, 1314, 1446, 1524), and a device (1126, 1526) for reversibly locking the removal wire (1128, 1358, 1414) of the intrauterine system. The proximal end of the measuring tube (1106, 1440, 1506) is movably attached to the distal end of the handle body (1108, 1330, 1454, 1508), provided that the measuring tube is arranged to remain lateral to the cervical canal during insertion. A plunger is movably arranged inside the handle body and the measuring tube. This disclosure also provides a kit including an insert and an intrauterine system.

The application discloses a novel uterus lifting device and a using method, which comprises a control handle, a hollow rod, a connecting rod, a cervical clamp and a uterus lifting cup. A tightening device is arranged in the uterus lifting cup. The tightening device comprises an elastic collar. The elastic collar is arranged in the center of the uterus lifting cup. The elastic collar is provided with an opening for tightening the outlet of the cervical canal. The cervical clamp can be retracted or extended from the cervical cup. First, the cervical clamp is extended from the cervical cup to clamp the cervix. Then, the cervical clamp clamps the cervix and is pulled down to the inside of the uterus lifting cup. At the same time, the elastic collar is used to tighten the opening of the cervical canal, so as to prevent the tissues in the uterine cavity, especially cancer tissues, from flowing out of the cervical canal, thereby preventing the further spread of cancer cells.

An inserter (1100, 1300, 1400, 1500) for an intrauterine system (1102, 1336, 1402, 1502) is described, comprising a handle body (1104, 1306, 1416, 1504), a measuring tube (1110, 1328, 1406, 1510), a plunger (1132, 1202, 1362, 1450, 1532), a flange (1122, 1404, 1522), a finger support (1124, 1314, 1446, 1524), and a means (1126, 1526) for reversibly locking the withdrawal thread (1128, 1358, 1414) of the system intrauterine. A proximal end (1106, 1440, 1506) of the measuring tube is movably attached to a distal end (1108, 1330, 1454, 1508) of the handle body, and the measuring tube is arranged to remain outside the cervical canal during insertion. The plunger is movably arranged within the handle body and the measuring tube. The present invention also provides a kit comprising the inserter and the intrauterine system.

A subendometrial injection device comprises a supporting sleeve, an injection sheath and an injection needle. The injection sheath is inserted into the supporting sleeve in a sliding mode, a positioning disc with the outer diameter larger than that of a cervix uteri outer opening is fixed to the outer wall of the supporting sleeve, the supporting sleeve is divided into an insertion section with the outer diameter smaller than the inner diameter of a cervix uteri tube and the length larger than that of the cervix uteri tube and a positioning section outside the cervix uteri, and the end, inserted into the supporting sleeve, of the injection sheath is an in-vivo section; and the other end extends out of the positioning section of the supporting sleeve to form an in-vitro section. An external thread section is arranged on the in-vitro section of the injection sheath, a first positioning nut used for positioning the insertion depth of the injection sheath is connected to the external thread section, an injection needle is movably inserted into the injection sheath, a first scale and a second scale which display the insertion depth of the injection sheath and the injection needle are arranged outside the injection sheath and the injection needle respectively, and the injection sheath is provided with a channel for injection of the bottom and the side wall of a uterine cavity. By adopting the device, multi-site subendometrial injection can be completed, the operation process is simple, the trauma is small, the risk is low, the injection depth can be accurately controlled, and clinical development is facilitated.

This invention relates to the field of ultrasound imaging diagnostic technology, and discloses a method and system for diagnosing adenomyosis based on multi-parameter ultrasound imaging of the cervix. The method utilizes a transvaginal probe to acquire two-dimensional grayscale, shear wave elasticity, and ultra-micro blood flow images of the cervix. An anatomical coordinate system is established based on the longitudinal axis of the cervical canal in the grayscale image, and multiple independent quantitative analysis sub-regions covering the internal os and mid-segment of the cervix are identified as measurement target areas within the cervical parenchyma. Young's modulus, reflecting tissue stiffness, and resistance index, reflecting microcirculatory resistance, are extracted from the elasticity and blood flow images, respectively. The extracted parameters are input into a multivariate logistic regression diagnostic model, and the probability value of disease risk is calculated based on weighted coefficients, outputting a classification conclusion. This invention overcomes the limitations of morphological diagnosis through a standardized target area localization strategy and multi-modal parameter joint modeling, achieving objective quantitative diagnosis of adenomyosis and improving the accuracy and repeatability of detection.

A puncture guide cannula effectively solves the problems that when an existing puncture needle enters a uterine cavity from a cervical canal, the wall of the cervical canal and the muscular wall of the uterine cavity are prone to being touched, needle inserting is difficult, and working efficiency is reduced. Comprising a sleeve in the left-right axial direction, the front side of the sleeve is provided with a notch which is through in the left-right direction and the inside-outside direction, the left side of the sleeve is provided with a plurality of receding grooves which are provided with leftward openings and distributed along the outer edge face of the sleeve, and a pin shaft perpendicular to the axis of the sleeve is fixed in each receding groove and rotationally connected with an inverted-L-shaped bent rod; the free end of the bent rod leftwards extends out of the sleeve and is fixedly provided with an arc-shaped plate; the intrauterine device is ingenious in structure and convenient to use, the tip of a puncture needle can be guided and protected when entering a uterine cavity, the tip of the puncture needle is prevented from making contact with the wall of a cervical canal and the wall of the uterine cavity muscle, the needle inserting process can be conducted smoothly, the inverted-L-shaped rod is pulled rightwards so that the arc-shaped plates can be opened, the cannula can be moved rightwards and pulled backwards, and the puncture needle can be inserted into the uterine cavity. And the sleeve can be conveniently taken off from the puncture needle, and is simple to operate and easy to popularize and use.

The present application relates to the technical field of medical devices, in particular to a cervical canal polypus resecter, comprising a handle, a mirror body fixedly connected to the handle, a base detachably connected to the end of the mirror body away from the handle, and a cutting mechanism for resecting polypus arranged on the base; a fixing mechanism for adsorbing and fixing polypus and a flushing mechanism for providing flushing liquid to the surgical area are arranged in the handle. When the cutting mechanism is unfolded, the fixing mechanism generates negative pressure to fix the polypus, and the flushing mechanism transmits the flushing liquid to the surgical area; when the cutting mechanism is closed, the fixing mechanism continuously fixes the polypus, and the flushing mechanism sucks the flushing liquid into the transmission area. The present application is used for simplifying the surgical operation and improving the fluency and safety of the operation.

The application provides an instrument tube, a sampling swab and a gynecological uterine cavity fungus sampling method. The application comprises an instrument tube body. The instrument tube can be extended into, expanded, attached to and supported the isolated cervical canal wall. After the instrument tube is used to explore and expand the cervix, the closed distal end can be cut off, and the instrument tube is converted into a double-end open instrument tube. The sampling swab can be extended into the channel of the instrument tube, pass through the distal end of the instrument channel supported by the mechanical tube and reach the uterine cavity to sample the uterine cavity fungus, so that the uterine cavity fungus sample is taken out through the sampling instrument tube channel. Compared with the prior art, the application greatly reduces the pollution opportunity of the uterine cavity fungus sample and improves the accuracy of the bacterial sampling result.

1. Name of the product in this design: Hysteroscopy. 2. Purpose of this design: for the examination, diagnosis and treatment of the cervical canal or uterine cavity. 3. The key design feature of this product is its shape. 4. The image or photograph that best illustrates the design's key points: 3D view 1.