30 results about "Tamponade" patented technology

An expandable tamponade for treating penetrating wounds comprises a balloon 104, wherein the balloon can be inflated to provide pressure onto the wound when the tamponade has been inserted into the wo

The present application relates to a kind of nasal balloon catheter and preparation method, the nasal balloon catheter includes expansion body and with expansion body communication injection part;The expansion body includes positioning fixed structure and expansion structure, positioning fixed structure can be supported in the nasal cavity of target object, expansion structure can be converted from shrink configuration to expansion configuration when injection filling medium in injection part;In expansion configuration, the expansion body matches with the internal physiological structure of the nasal cavity of target object;At least one ventilation catheter is provided in the expansion body, the inner cavity of ventilation catheter is ventilation passage, one end of ventilation passage is communicated with external atmosphere, the other end is communicated with nasal cavity internal airway.Compared with prior art, the present application solves the problems of inaccurate reduction, large damage in existing nasal bone fracture treatment, incomplete compression of nasal bleeding, low comfort level caused by nasal postoperative tamponade, poor effect of nasal cavity narrow treatment method, nasal cavity tamponade while unable to drain and clean nasal cavity and the like.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent.

A conformable surgical tampon for disposition into and removal from an anatomical cavity of a mammalian patient by a doctor to absorb and collect bodily fluids. The tampon comprises an absorbent chassis material and a plurality of spaced apart positioning strings attached to the chassis. The spaced apart positioning strings are operative to selectively position the conformable nasopharyngeal tampon within an anatomical cavity of a patient responsive to manipulation of a positioning string by a surgeon. The tampon is particularly suited for nasopharyngeal surgery.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent.

Disclosed is a pediatric emergency kit for esophageal tamponade procedures in pediatric patients and methods of use thereof. The pediatric emergency kit includes at least one esophageal balloon catheter for the tamponade of blood flow, and an inflation hand pump equipped with a pressure gauge for inflating a balloon on the balloon catheter. The pediatric emergency kit can be configured to include multiple compartments, optionally, with a first container / compartment containing at least the esophageal balloon catheter and a second container / compartment containing at least the inflation handpump, and optionally a second esophageal balloon catheter. Optionally, both the first and second containers / compartments contain a syringe, a 3-way luer lock stopcock, and / or a guidewire. Also provided are instructions and / or methods of using the kit for correct placement and inflation of the esophageal balloon to effectively manage arterio-esophageal fistulas.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent.

The present application relates to a kind of hemangioma occlusion device, hemangioma occlusion treatment device and hemangioma occlusion system, hemangioma occlusion device includes mesh expansion structure and guide structure, the mesh expansion structure has from the unwinding state of spiral shape around from distal end to proximal end and the compressed state for being delivered from inside blood vessel to hemangioma;At least a part of the guide structure is arranged in the lumen of mesh expansion structure, and when the mesh expansion structure is in spiral shape, at least a part of the guide structure is unwound in the lumen of mesh expansion structure in spiral shape.The present application has the advantages of preventing hemangioma rupture, preventing vascular embolism, improving the coverage of tumor neck, promoting the formation of intratumoral thrombus, accelerating hemangioma embolism and the like while realizing stable and compliant tamponade.

A tampon product and method are presented that includes an applicator including an outer member and an inner member slidably engaged with the outer member. The outer member includes an outer surface surrounding a longitudinal axis, a grip region, an insertion region, and an intermediate region. The grip region includes an inverted region such that a portion of the grip region is adjacent to the inner surface of the cylindrical paper segment, and a pusher opening is internal to the cylindrical paper segment.

A tampon product including a tampon within an applicator assembly is disclosed. The applicator assembly includes a barrel portion joined to a gripping portion, imparted with features that improve utility and convenience for the user. In one example the gripping portion has a rearward edge defining differing first and second lengths. In another example the gripping portion has a lateral outer cross section profile that is substantially oval-shaped, ovoid-shaped, elliptical or stadium-shaped and has major and minor axes, each perpendicular to a longitudinal axis, along first and second lateral perpendicular directions, wherein following absorption of fluid the tampon will expand laterally to a first lateral dimension to a greatest extent along a first lateral direction, and to a lesser second lateral dimension along a second lateral direction 90 degrees from the first lateral direction, wherein the first lateral direction is substantially parallel to one of the major and minor axes.

The invention discloses double-air-bag compression and ICG injection type nasal cavity hemostasis equipment, and relates to the technical field of medical instruments, the double-air-bag compression and ICG injection type nasal cavity hemostasis equipment comprises a tube body assembly and an inflation assembly, the tube body assembly comprises a straight tube and an arc tube, the outer surface of the arc tube is fixedly wrapped with a rear nasal cavity air bag, the outer surface of the straight tube is fixedly wrapped with a front nasal cavity air bag, and the front nasal cavity air bag is fixedly wrapped with a rear nasal cavity air bag. The inflation assembly can inflate the front nasal cavity air bag and the rear nasal cavity air bag. According to the double-air-bag compression and ICG injection type nasal cavity hemostasis equipment, the double-air-bag compression and ICG injection type nasal cavity hemostasis equipment is provided with a double-air-bag independent pressure measuring system, partitioned pressure independent regulation and control are achieved through the front nasal cavity air bag and the rear nasal cavity air bag respectively, compared with traditional empirical filling, the pressure stability can be improved, and when a tube is pulled out, the operation is easy, and the operation is convenient. The gradual pressure reduction is combined with real-time observation of an endoscope, so that the risk of secondary bleeding is reduced, and meanwhile, the ischemic necrosis rate of the mucous membrane flap is also reduced.

The utility model relates to the technical field of tracheal catheter fixing devices, and discloses an intraoral special-shaped inflatable cuff tracheal catheter fixing device, which comprises a main joint, a connector and a tracheal catheter main body, a middle shaft part is arranged outside the tracheal catheter main body, and an air inlet nozzle is mounted on the left side of the top of a cuff. According to the utility model, the gap groove is formed in the center of the middle shaft part, so that the tracheal catheter main body can penetrate through the gap groove, when the middle shaft part is assembled, the middle shaft part can be surrounded outside the tracheal catheter main body, and under the elastic compression of the clamping spring, the clamping plate can be used for clamping the outside of the tracheal catheter main body; the position of the cuff can be adjusted by adjusting the position of the cuff, then the mounting piece is used for locking the position, and the cuff is gradually expanded and inflated by utilizing the inflating work of the inflating injector, so that the tracheal catheter main body is fixed in the oral cavity in an inflating and filling manner, no any tissue damage is caused, an adhesive tape is not needed, and the tracheal catheter main body is firm in fixation, not easy to shift, safe and efficient.

The present disclosure relates to a tamponade device. The tamponade device includes a sheath member. The sheath member includes a hollow cavity defined along a length of the sheath member. The hollow cavity is configured to allow the insertion of a guidewire therein. The sheath member is configured to be positioned at a vascular access point of a subject over a guidewire deployed into the lumen of a blood vessel at the vascular access site. Further, the sheath member is configured with a predefined diametrical size that impedes the tamponade device from being deployed into the lumen of the blood vessel through the vascular access point, thereby positioning the sheath member at the vascular access point to occlude the vascular access point. By applying focal pressure or compression to the blood vessel directly at the vascular access site, hemostasis can be achieved using the tamponade device.

A tampon product and method are presented that includes an applicator including an outer member and an inner member slidably engaged with the outer member. The outer member includes an outer surface surrounding a longitudinal axis and a grip region, an intermediate region, and an insertion region. The grip region includes an inverted region such that a portion of a wall of the grip end region is adjacent to the inner surface of the cylindrical paper segment, and a pusher opening internal to the cylindrical paper segment.

A tampon product and method are presented that includes an applicator including an outer member and an inner member slidably engaged with the outer member. The outer member includes an outer surface surrounding a longitudinal axis, a grip region, an insertion region, and an intermediate region. The grip region includes an inverted region such that a portion of the grip region is adjacent to the inner surface of the cylindrical paper segment, and a pusher opening is internal to the cylindrical paper segment.

An intravaginal apparatus comprising a bullet-shaped body with outer, middle mesh, and inner layers is provided. The device is configured to contain insertable materials such as tampons, absorbents, drugs, or therapeutic compounds. One or more openings, optionally fitted with mesh guards, enable fluid exchange and adsorption of pathogens and odor-causing compounds. In some embodiments, the insertable material includes activated carbon engineered to adsorb volatile amines and indoxyl sulfate and may release therapeutic agents in response to microbial presence. The apparatus may preserve vaginal pH and microbiota, support directional fluid flow, and be suitable for single-use or extended wear. Applications include treatment and prevention of vaginal infections such as bacterial vaginosis and toxic shock syndrome.

A tampon including a pledget, a wicking member disposed in direct contact with the pledget, and a withdrawal cord is disclosed. The wicking member is non-coaxially arranged with respect to the withdrawal cord.

This utility model discloses a bladder irrigation device, relating to the field of medical device technology. It includes a bladder irrigation catheter, a negative pressure suction catheter, a negative pressure suction mechanism, and an endoscope mechanism. The front end of the bladder irrigation catheter is inserted into the bladder to be treated, and a flushing water inlet is provided on the rear side wall of the bladder irrigation catheter. The negative pressure suction catheter can be inserted into the bladder irrigation catheter, and a flushing water channel can be formed between the outer wall of the negative pressure suction catheter and the inner wall of the bladder irrigation catheter. The front end of the flushing water channel is open to flush the bladder to be treated, and the rear end of the flushing water channel is closed. The inlet of the negative pressure suction mechanism can communicate with the rear end of the negative pressure suction catheter to drain the bladder to be treated. The probe of the endoscope mechanism can be inserted into the bladder irrigation catheter to take images inside the bladder to be treated. This utility model can achieve bedside visual negative pressure bladder irrigation, improving the treatment effect of bladder tamponade.

The present invention introduces a tampon with an integrated device designed for improved insertion, and removal, and leak prevention. The device comprises a flexible, nonpermeable wall, hollow to enable finger-assisted insertion and featuring a removal aid element attached to the bottom end of the wall for easy, hygienic extraction. Additionally, the wall is equipped with ridges that conform to the vaginal wall, enhancing the seal to prevent menstrual fluid leakage and block the absorption of external fluids. In other embodiments, a smoothed wall is offered. This invention eliminates the need for separate applicators, allows the device to compact for discrete portability, and significantly enhances user comfort and effectiveness in fluid management.

A tampon product and method are presented that includes an applicator including an outer member and an inner member slidably engaged with the outer member. The outer member includes an outer surface surrounding a longitudinal axis and a grip region, an intermediate region, and an insertion region. The grip region includes an inverted region such that a portion of a wall of the grip end region is adjacent to the inner surface of the cylindrical paper segment, and a pusher opening internal to the cylindrical paper segment.

This utility model relates to the field of skincare product packaging technology and discloses an eye mask bagging device, including a frame, an eye mask conveying unit, a packaging bag conveying unit, a flaring unit, a lifting unit, and a pushing unit. The eye mask conveying unit, the lifting unit, and the flaring unit are sequentially connected within the frame along its length. The eye mask conveying unit conveys the eye mask to the lifting unit. The pushing unit and the packaging bag conveying unit are sequentially connected to the frame along the conveying direction of the conveying unit, with the packaging bag conveying unit located above the flaring unit. The packaging bag conveying unit conveys the packaging bag to the top of the flaring unit and cooperates with the flaring unit to open the bag opening. The eye mask located on the lifting unit is lifted to the front of the packaging bag opening by the lifting unit, and the pushing unit pushes the eye mask located in front of the packaging bag opening into the corresponding packaging bag. This utility model can convey eye masks into packaging bags, automate packaging, and improve efficiency.

The invention is a tampon assembly for a woman. The tampon assembly has a tampon with a string attached thereto for insertion into the woman, a base for attaching to the tampon, wherein the base has: one or more catches to contain a string from a tampon, a thread to receive the string which is wound around the thread and a magnet in the base. The assembly also has a magnetic retrieval tool for attracting the magnet in the base to retrieve and insert the tampon inside of the woman.

A tampon having an insertion end and a withdrawal end. The tampon includes a primary absorbent, disposed toward the insertion end, a secondary absorbent, and a withdrawal member. The secondary absorbent may have a mean length from the primary absorbent and at least three segments each having a mean segment mass. The mean segment mass may be selected such that the secondary absorbent tapers as the secondary absorbent material extends from the primary absorbent.

A vitreous humor filling agent for the posterior space in the eye comprises at least one structurally asymmetric fluoroether which is in a liquid state at room temperature or under surgical conditions and which can be converted to a gaseous state after injection into the eye as a result of its own intrinsic vapour pressure or by means of an external non-invasive method. In addition to the above requirements, such compounds also have a specific gravity of between 1.1 and 1.6 (the latter being an upper limit to prevent retinal toxicity), are immiscible with water, are non-flammable, have high ultrasound absorption, and are in a clear colourless form.

The application discloses a silicone oil filling simulation method and device for assisting treatment of retinal detachment, and the method comprises the following steps: constructing an eyeball wall model of a patient according to an elastic solid modeling method, and maintaining the incompressibility of the eyeball wall by adopting an implicit iterative correction pressure method based on the number density; for the scene of filling silicone oil in the intraocular cavity during surgery, the silicone oil is regarded as a high-viscosity incompressible Newton fluid, and the interaction between the silicone oil and the eyeball wall is simulated according to the coupling method between the fluid and the elastic solid; and the three-phase coupling environment composed of water, silicone oil and the eyeball wall generated by the aqueous humor entering the vitreous cavity after surgery is simulated, and the emulsification phenomenon of the water and the silicone oil occurring at the immiscible boundary is simulated. According to the technical scheme of the application, the eyeball wall is constructed according to the elastic solid modeling method, the filling environment is visualized, and the dynamic interaction generated by the filling is simulated through the volume incompressible model based on the number density, so that accurate quantitative analysis can be provided for the surgical treatment.

A tamponade biological material for hemostasis and a preparation method therefor. The tamponade biological material is obtained by pretreating, crosslinking, and post-treating a small intestinal submucosal material. The tamponade biological material has good water resistance, a low swelling rate, and an appropriate degradation speed; it is degradable and not prone to adhesion and curling, thereby avoiding wound traction and reducing patient pain, so it is suitable for hemostasis in various situations, and has good market application prospects.

The application belongs to the field of medical devices, and particularly relates to a negative pressure uterine cavity tamponade hemostasis device, which comprises a cannula body, a suction head connected to the front end of the cannula body, a capsule body sleeved on the outside of the cannula body, and an inflation tube connected to the capsule body for inflating or filling the capsule body with liquid; the suction head is located in front of the capsule body, and the suction head is provided with a plurality of suction holes communicating with the inner cavity of the suction head. The application is convenient to operate, changes the traditional hemostasis mode of filling and cooperating with a uterine contraction needle, and is completely consistent with the principle of uterine contraction in physics and physiology to contract the uterine cavity through negative pressure suction so as to achieve better direct uterine contraction effect as soon as possible, and greatly improves the hemostasis effect.

A gastroesophageal tamponade and method of using a gastroesophageal tamponade involves illuminating a trachea and an esophagus of a subject with light from a distal end of the tamponade. In one implementation, the gastroesophageal tamponade comprises a body extending from a proximal end to a distal end. The body has an outer perimeter and a guide lumen extending at least partially through the body. The body comprises an aspiration lumen located at least partially between the guide lumen and the outer perimeter and an inflation lumen located at least partially between the guide lumen and the outer perimeter. A balloon extends at least partially around the body.

Multiple, separable disposal bags for tampons and pads are wrapped around a center roll. Each bag is connected to the next bag on the roll by a seam that includes a slit and a series of perforations separating connection points between the bags. A bag tail secures the first bag to itself by a bag tail that has an adhesive portion and a free, tab portion. The adhesive portion is attached to the first bag at a first zone and to a different portion of the first bag at a second zone. A user can pull on the free-tab portion of the bag tail to detach the second zone of the adhesive portion from the first bag. The first zone of the adhesive portion remains attached to the first bag after the first bag is detached from the subsequent bag at their seam.

The object of the invention is an external tampon characterized in that it has the shape of an elongated spindle and its cross-section has the shape of a circle or an oval, wherein it comprises three adjacent parts (A, B, C), wherein the second part (B) of the tampon is located between two tapering parts (A, C) of which the first part (A) is shorter and represents about 23% of the total length of the tampon and the third part (C) is longer with respect to the first part (A) and represents about 50% of the total length of the tampon, wherein the tampon is made of an absorbent filling covered on its entire surface with a fluid-permeable material.