A maintenance bag of an ostomy system can include fewer sensors than a diagnostic or analytic ostomy bag that is typically used for newer users. The maintenance bag can include sensors and electronics to detect fill level of the bag. The maintenance bag can also include a bag sealing mechanism that can detect drainage events and help the user to track inventory of the bags. A wafer that can be used with an ostomy bag can include leak sensors configured to detect leak of effluent via a single opening in the hydrocolloid layer that interfaces with skin of a user. The wafer can also include temperature sensors configured to detect inflammation. The wafer can further include a convex interface for better fit with certain users.
A coupling assembly for an ostomy appliance that has a bag side flange having a bag and an integrated element having an accordion membrane and a body side flange, the integrated element configured to be selectively coupled to the bag side flange. The integrated element is formed in a single manufacturing process.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
B29C 45/14 - Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mouldApparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
A method for identifying urological health information. The method includes storing user-defined inputs provided by a user, monitoring a fluid volume of urine processed by the user, storing parameters regarding the fluid volume of urine, utilizing a machine learning algorithm to provide processed data based on the user-defined inputs and stored parameters, and providing feedback based on the processed data.
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
An apparatus according to certain embodiments generally includes an elongated tubular member having a proximal end and an opposite distal end, and an inflatable balloon surrounding the distal end. The elongated tubular member comprises an outer tube, a non-collapsible inner tube positioned within the outer tube, and a compressible material positioned between the outer tube and the inner tube.
The appliance comprises a pouch having a vent aperture and a filter secured to the pouch with adhesive and covering the vent aperture. The filter includes an adhesive layer comprising the adhesive and an adsorbent layer. The filter also includes a gas permeable cover layer secured to the adhesive layer such that the adsorbent layer is covered by the gas permeable cover layer. The gas permeable cover layer has an outer profile and the adhesive layer has a corresponding outer profile which is in register with the outer profile of the gas permeable cover layer. The adsorbent layer is positioned on a first side of the adhesive layer so that a first portion of the first side of the adhesive layer is not covered by the adsorbent layer and the gas permeable cover layer is secured to the first portion of the first side of the adhesive layer.
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
An ostomy appliance comprises a pouch and a drain. The drain is formed of two walls attached to one another lateral edges to define a channel therebetween and comprises pursing strips to separate the walls when compressed in a direction perpendicular to the lateral edges of the drain. A pursing strip comprises a transverse edge perpendicular to the lateral edges and the transverse edge comprises a notch spanning at least half of the transverse edge. A pursing strip may comprise a line of weakness. The line of weakness may span between side edges of the pursing strip. The line of weakness may be curved. A pursing strip may comprise two converging lines of weakness spanning between upper and lower edges of the pursing strip. The drain may comprise two or three pursing strips. A gap may be provided between pursing strips.
Methods of modifying a medical device and manufacturing a medical device are disclosed. One embodiment of a method of modifying a medical device includes treating a portion of the medical device with cold plasma and functionalizing the plasma-treated portion with a polymer. One embodiment of a method of manufacturing a medical device includes providing a subcutaneous part configured to be positioned subcutaneously in a user and performing a surface treatment on a portion of the subcutaneous part.
B05D 3/14 - Pretreatment of surfaces to which liquids or other fluent materials are to be appliedAfter-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by electrical means
Embodiments described herein relate to compounds for the detection of wounds, e.g., chronic wounds or infected wounds, including compositions, substrates, kits, dressing materials, and articles, and systems containing such compounds. Further embodiments relate to methods of using these compositions, kits and systems in diagnostic assays, and in the diagnosis and/or detection of chronic or infected wounds based on enzymatic conversion of specific substrates which are contained in the compositions. Additional embodiments relate to methods of characterizing wounds based on expression of a plurality of markers and using such information to treat, manage, and follow-up patients suffering from chronic or infected wounds.
A method for controlling a medical device. The method includes providing a conduit coupled to a pump, the pump configured to selectively provide a pressure in the conduit, a motor configured to selectively drive the pump at an operating frequency to provide the pressure in the conduit, and a controller configured to selectively drive the motor and monitor the medical device. The method includes selectively driving the motor at an indicating frequency that is different from the operating frequency when the controller identifies a value outside of a threshold for the medical device. The indicating frequency produces an indicating audible or haptic feedback that is greater than an operating audible or haptic feedback provided at the operating frequency.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
Systems and methods of providing post-operative ostomy patient care can include software and/or hardware that facilitates patient care personnel, such as a patient coach, providing remote patient care or coaching over a network to an ostomy patient. The care may be provided by specially trained former patients, nurses, or other care providers. The system can integrate sensor data from an ostomy device and inputs from the former patients, healthcare professionals, and/or device manufacturer in provide the post-operative care.
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
G16H 20/40 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilitiesICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
G16H 80/00 - ICT specially adapted for facilitating communication between medical practitioners or patients, e.g. for collaborative diagnosis, therapy or health monitoring
Certain embodiments of the present application relate to an adjustable ostomy wafer system including an ostomy wafer and an insert ring. The ostomy wafer includes an adjustable layer with an effluent opening through which effluent flows, and the adjustable layer has a body-facing side and a non-body-facing side. The insert ring is capable of providing or increasing convexity of the adjustable layer when the insert ring is pressed against the non-body-facing side of the adjustable layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A maintenance bag of an ostomy system can include fewer sensors than a diagnostic or analytic ostomy bag that is typically used for newer users. The maintenance bag can include sensors and electronics to detect fill level of the bag. The maintenance bag can also include a bag sealing mechanism that can detect drainage events and aid the user to track inventory of the bags. A wafer that can be used with an ostomy bag can include leak sensors configured to detect leak of effluent via a single opening in the hydrocolloid layer that interfaces with skin of a user. The wafer can also include temperature sensors configured to detect inflammation. The wafer can further include a convex interface for better fit with certain users.
A61F 5/449 - Body securing means, e.g. belts, garments
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 13/42 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators with wetness indicator or alarm
13.
Ostomy wafers incorporating adhesives and foam layers, ostomy devices including the same, and methods of applying ostomy wafers and ostomy devices
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed. An ostomy wafer may include an external layer and a convex surface coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex surface coupled to the external layer.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01K 3/10 - Thermometers giving results other than momentary value of temperature giving differences of valuesThermometers giving results other than momentary value of temperature giving differentiated values in respect of time, e.g. reacting only to a quick change of temperature
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
A method for identifying urological health information. The method includes storing user-defined inputs provided by a user, monitoring a fluid volume of urine processed by the user, storing parameters regarding the fluid volume of urine, utilizing a machine learning algorithm to provide processed data based on the user-defined inputs and stored parameters, and providing feedback based on the processed data.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex surface coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex surface coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A rectal drainage appliance is disclosed comprising a tubular element having an inflatable balloon at a distal end for anchoring the appliance in the rectum. The appliance includes one or more of: (i) first and second auxiliary lumens communicating with the inflatable balloon to provide independent inflation and pressure monitoring paths coupled to the balloon; (ii) a pressure state indicator defined by a mechanical element configured to flip between first and second states or shapes responsive to sensed pressure; and (iii) a collapsible auxiliary lumen larger than the inflation lumen, and configured to permit admission of irrigation fluid. The pressure state indicator may also be used in intestinal drains.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 25/04 - Holding devices, e.g. on the body in the body, e.g. expansible
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01K 3/10 - Thermometers giving results other than momentary value of temperature giving differences of valuesThermometers giving results other than momentary value of temperature giving differentiated values in respect of time, e.g. reacting only to a quick change of temperature
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
G01D 5/24 - Mechanical means for transferring the output of a sensing memberMeans for converting the output of a sensing member to another variable where the form or nature of the sensing member does not constrain the means for convertingTransducers not specially adapted for a specific variable using electric or magnetic means influencing the magnitude of a current or voltage by varying capacitance
G01K 13/00 - Thermometers specially adapted for specific purposes
20.
Surface treatment system and method for subcutaneous device
Methods of modifying a medical device and manufacturing a medical device are disclosed. One embodiment of a method of modifying a medical device includes treating a portion of the medical device with cold plasma and functionalizing the plasma-treated portion with a polymer. One embodiment of a method of manufacturing a medical device includes providing a subcutaneous part configured to be positioned subcutaneously in a user and performing a surface treatment on a portion of the subcutaneous part.
A61L 24/00 - Surgical adhesives or cementsAdhesives for colostomy devices
B05D 3/14 - Pretreatment of surfaces to which liquids or other fluent materials are to be appliedAfter-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by electrical means
Systems and methods of providing post-operative ostomy patient care can include software and/or hardware that facilitates patient care personnel, such as a patient coach, providing remote patient care or coaching over a network to an ostomy patient. The care may be provided by specially trained former patients, nurses, or other care providers. The system can integrate sensor data from an ostomy device and inputs from the former patients, healthcare professionals, and/or device manufacturer in provide the post-operative care.
G08B 5/00 - Visible signalling systems, e.g. personal calling systems, remote indication of seats occupied
H05B 39/00 - Circuit arrangements or apparatus for operating incandescent light sources
H05B 41/00 - Circuit arrangements or apparatus for igniting or operating discharge lamps
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
G16H 20/40 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to mechanical, radiation or invasive therapies, e.g. surgery, laser therapy, dialysis or acupuncture
G16H 80/00 - ICT specially adapted for facilitating communication between medical practitioners or patients, e.g. for collaborative diagnosis, therapy or health monitoring
G16H 40/67 - ICT specially adapted for the management or administration of healthcare resources or facilitiesICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
22.
WOUND DRESSING COMPRISING AN ANTIMICROBIAL COMPOSITION
Methods, processes and compositions are provided for improved wound dressings comprising an antimicrobial composition. The wound dressings maintain conformability and strength, as well as antimicrobial performance, upon use after storage.
A61L 15/20 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
A61L 15/46 - Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
A61L 15/18 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
An apparatus according to certain embodiments generally includes an elongated tubular member having a proximal end and an opposite distal end, and an inflatable balloon surrounding the distal end. The elongated tubular member comprises an outer tube, a non-collapsible inner tube positioned within the outer tube, and a compressible material positioned between the outer tube and the inner tube.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/442 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having irrigation ports or means
Methods of modifying a medical device and manufacturing a medical device are disclosed. One embodiment of a method of modifying a medical device includes treating a portion of the medical device with cold plasma and functionalizing the plasma-treated portion with a polymer. One embodiment of a method of manufacturing a medical device includes providing a subcutaneous part configured to be positioned subcutaneously in a user and performing a surface treatment on a portion of the subcutaneous part.
Methods of modifying medical devices and medical devices are disclosed, One embodiment of a method of modifying a medical device includes functionalizing a surface of the medical device using cold plasma. One embodiment of a medical device is obtained by a method of modifying a device that includes functionalizing a surface of the medical device using cold plasma.
A coupling assembly for an ostomy appliance that has a bag side flange having a bag and an integrated element having an accordion membrane and a body side flange, the integrated element configured to be selectively coupled to the bag side flange. The integrated element is formed in a single manufacturing process.
Methods of modifying medical devices and medical devices are disclosed, One embodiment of a method of modifying a medical device includes functionalizing a surface of the medical device using cold plasma. One embodiment of a medical device is obtained by a method of modifying a device that includes functionalizing a surface of the medical device using cold plasma.
A coupling assembly for an ostomy appliance that has a bag side flange having a bag and an integrated element having an accordion membrane and a body side flange, the integrated element configured to be selectively coupled to the bag side flange. The integrated element is formed in a single manufacturing process.
An apparatus according to certain embodiments generally includes an elongated tubular member having a proximal end and an opposite distal end, and an inflatable balloon surrounding the distal end. The elongated tubular member comprises an outer tube, a non-collapsible inner tube positioned within the outer tube, and a compressible material positioned between the outer tube and the inner tube.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/442 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having irrigation ports or means
Methods of modifying a medical device and manufacturing a medical device are disclosed. One embodiment of a method of modifying a medical device includes treating a portion of the medical device with cold plasma and functionalizing the plasma-treated portion with a polymer. One embodiment of a method of manufacturing a medical device includes providing a subcutaneous part configured to be positioned subcutaneously in a user and performing a surface treatment on a portion of the subcutaneous part.
A61L 31/16 - Biologically active materials, e.g. therapeutic substances
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
A coupling assembly for an ostomy appliance that has a bag side flange having a bag and an integrated element having an accordion membrane and a body side flange, the integrated element configured to be selectively coupled to the bag side flange. The integrated element is formed in a single manufacturing process.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
B29C 45/14 - Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mouldApparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
An apparatus according to certain embodiments generally includes an elongated tubular member having a proximal end and an opposite distal end, and an inflatable balloon surrounding the distal end. The elongated tubular member comprises an outer tube, a non-collapsible inner tube positioned within the outer tube, and a compressible material positioned between the outer tube and the inner tube.
Methods of modifying medical devices and medical devices are disclosed. One embodiment of a method of modifying a medical device includes functionalizing a surface of the medical device using cold plasma. One embodiment of a medical device is obtained by a method of modifying a device that includes functionalizing a surface of the medical device using cold plasma.
B05D 1/00 - Processes for applying liquids or other fluent materials
B05D 5/02 - Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain a matt or rough surface
B05D 3/14 - Pretreatment of surfaces to which liquids or other fluent materials are to be appliedAfter-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by electrical means
A fluid collection apparatus for use in negative pressure wound therapy. The fluid collection apparatus includes a flexible bag having a first opening and a second opening. The bag includes a structure defining a fluid pathway connecting the first opening and the second opening. The pathway is circulative and contributes to orientation independence of the bag in use. The bag further includes a load-bearing component.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A maintenance bag of an ostomy system can include fewer sensors than a diagnostic or analytic ostomy bag that is typically used for newer users. The maintenance bag can include sensors and electronics to detect fill level of the bag. The maintenance bag can also include a bag sealing mechanism that can detect drainage events and aid the user to track inventory of the bags. A wafer that can be used with an ostomy bag can include leak sensors configured to detect leak of effluent. The wafer can also include temperature sensors configured to detect inflammation. The wafer can further include a convex interface for better fit with certain users.
A maintenance bag of an ostomy system can include fewer sensors than a diagnostic or analytic ostomy bag that is typically used for newer users. The maintenance bag can include sensors and electronics to detect fill level of the bag. The maintenance bag can also include a bag sealing mechanism that can detect drainage events and aid the user to track inventory of the bags. A wafer that can be used with an ostomy bag can include leak sensors configured to detect leak of effluent. The wafer can also include temperature sensors configured to detect inflammation. The wafer can further include a convex interface for better fit with certain users.
Multi component fibres for the reduction of the damaging activity of wound exudate components such as protein degrading enzymes and inflammatory mediators in wounds, the fibres comprising: from 10% to 100% by weight of the fibres of pectin and a sacrificial proteinaceous material in a weight ratio of 100:0 to 10:90 pectin to sacrificial proteinaceous material and from 0% to 90% by weight of the fibres of another polysaccharide or a water soluble polymer.
A61L 15/22 - Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
D01F 8/02 - Conjugated, i.e. bi- or multicomponent, man-made filaments or the likeManufacture thereof from cellulose, cellulose derivatives, or proteins
B29C 48/88 - Thermal treatment of the stream of extruded material, e.g. cooling
A bag connector system includes a first coupling element, with a self-closing seal and a housing having a fluid inlet port and a fluid outlet port, and a second coupling element, with a housing having a fluid inlet end and a fluid outlet end. The fluid inlet end is configured to displace the self-closing seal when inserted into the fluid outlet port of the first coupling element. A bag connector system optionally includes a locking mechanism to maintain the first coupling element and second coupling element in a coupled state. Uncoupling of the first and second coupling elements results in minimal fluid contamination on the outer surfaces of the coupling elements. The bag connector systems provided herein are included in medical appliances for waste management.
F16L 37/38 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in only one of two pipe-end fittings
F16L 37/32 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in each of two pipe-end fittings at least one of two lift valves being opened automatically when the coupling is applied
A61M 39/26 - Valves closing automatically on disconnecting the line and opening on reconnection thereof
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
F16L 37/46 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in only one of two pipe-end fittings with a gate valve or sliding valve
39.
High barrier elastomer fecal catheter or ostomy pouch
Certain embodiments relate to a soft odor barrier material in a medical device. The soft odor barrier material includes an elastomer and an antiblocking agent. In certain forms, the antiblocking agent imparts an interior rough surface having an arithmetic mean surface roughness (Ra) not less than 0.1 μm. In certain forms, the antiblocking agent is non-blocking upon folding and packaging.
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
A stoma adapter is described that is especially suited to a recessed stoma or a flush stoma. The stoma adapter effectively extends the discharge passage from the stoma, protects peristomal skin, and forms a bridge at the interface between the stoma and an ostomy appliance. The stoma adapter contains a substantially unobstructed discharge passage, at least for effluent flowing in a discharge direction. The stoma adapter includes a seal for sealing against the bowel wall. The stoma adapter has collapsing, expanding, flexible and reinforced designs.
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
42.
COMPOSITION COMPRISING ANTIMICROBIAL METAL IONS AND A QUATERNARY CATIONIC SURFACTANT
The present invention relates to an antimicrobial composition suitable for use on skin and wounds comprising a source of an antimicrobial metal ion and a quaternary cationic surfactant.
A61K 31/14 - Quaternary ammonium compounds, e.g. edrophonium, choline
A01N 37/44 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio-analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio-analogue of a carboxylic group, e.g. amino-carboxylic acids
An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using optical sensors, e.g. spectral photometrical oximeters
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
Provided herein are microbial infection indicator devices, including dressing with indicators, standalone indicator inserts or disks that can be freely placed at a wound site or dressing, and applications thereof for displaying a visible or detectable signal to a user upon detection of an analyte or biomarker indicative of an infection, such as a color change.
G01N 33/00 - Investigating or analysing materials by specific methods not covered by groups
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
A61F 13/84 - Accessories, not otherwise provided for, for absorbent pads
C12Q 1/37 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving hydrolase involving peptidase or proteinase
An ostomy appliance according to certain embodiments generally includes a pouch, an adhesive collar, and a release liner. The adhesive collar includes an adhesive to secure the pouch around a stoma. The release liner is configured to allow manipulation of the adhesive through the pouch. The adhesive collar is attached to the pouch around a stomal opening for fitting around the stoma, and the adhesive in the adhesive collar is attached to an inside of the pouch.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
The application relates to an infusion part comprising a cannula part (7) and a fluid path, whereby a sealing (18) is positioned between the cannula part and the inlet/outlet opening (12) of the fluid path when the cannula part is in position for use in order to keep the fluid path to the cannula tight. The sealing (18) is surrounding the inlet/outlet opening (12) and/or the distance di between a centre line c of the cannula part and a point on the outer surface of the cannula part positioned at or above the upper edge of the sealing (18) is larger than the distance 02 between the centre line c of the cannula part and a point on the outer surface of the cannula part positioned at or below the lower edge of the sealing.
Embodiments described herein relate to compounds for the detection of wounds, e.g., chronic wounds or infected wounds, including compositions, substrates, kits, dressing materials, and articles, and systems containing such compounds. Further embodiments relate to methods of using these compositions, kits and systems in diagnostic assays, and in the diagnosis and/or detection of chronic or infected wounds based on enzymatic conversion of specific substrates which are contained in the compositions. Additional embodiments relate to methods of characterizing wounds based on expression of a plurality of markers and using such information to treat, manage, and follow-up patients suffering from chronic or infected wounds.
A medical device according to certain embodiments generally includes a first wall, a second wall, and a first deformable reinforcing member. The first wall and the second wall are joined to one another such that a cavity is formed between the first wall and the second wall. The cavity has an outlet opening formed at a proximal end of the medical device. The first deformable reinforcing member is attached to the first wall, and is deformable by manual application of pressure to lateral edges of the first deformable reinforcing member so as to radially distend the outlet opening. The first deformable reinforcing member includes at least one first notch formed in at least one lateral edge thereof. Each notch is configured to receive a portion of a user's digit to facilitate manual application of pressure to said lateral edges.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
A61F 5/442 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having irrigation ports or means
A miniaturized monitoring device can include electronic circuitry, housing, and communications protocols. The device can be a robust sensing device that can quantify electrolyte content accurately and transmit continuously from within fecal effluent or urine, or other human bodily fluid and/or solid samples. The device can be fully immersed in the testing sample, which can be in a container, an ostomy bag, or otherwise.
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61B 5/1477 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using chemical or electrochemical methods, e.g. by polarographic means non-invasive
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/1473 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using chemical or electrochemical methods, e.g. by polarographic means invasive, e.g. introduced into the body by a catheter
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
Valves and valve systems are provided that are useful for integration with inflatable indwelling medical devices to prevent over-inflation of retention balloon.
Urine collection bags, kits including urine collection bags, methods of collecting urine, and methods of manufacturing urine collection bags are disclosed herein. A urine collection bag includes an outer profile, an inner profile, and first and second external layers. The first and second external layers are sealed around a first periphery to define the inner profile. The inner profile has a container portion and an elongated portion.
Urine collection bags, kits including urine collection bags, methods of collecting urine, and methods of manufacturing urine collection bags are disclosed herein. A urine collection bag includes an outer profile, an inner profile, and first and second external layers. The first and second external layers are sealed around a first periphery to define the inner profile. The inner profile has a container portion and an elongated portion.
Urine collection bags, kits including urine collection bags, methods of collecting urine, and methods of manufacturing urine collection bags are disclosed herein. A urine collection bag includes an outer profile, an inner profile, and first and second external layers. The first and second external layers are sealed around a first periphery to define the inner profile. The inner profile has a container portion and an elongated portion.
A method for determining the hydration status of a person prompts the person to breathe while in a first postural position during which the method measures a first heart rate variability (HRV) value. The person is prompted to change to a second postural position, and the method measures a second HRV value. A difference between the first HRV value and the second HRV value is a daily score. The daily score is subtracted from a baseline to obtain a hydration score. In certain embodiments, the person is requested to respond to a plurality of subjective questions. The method processes the subjective responses and the daily score to determine whether the person is adequately hydrated. In certain embodiments of the method, the person is requested to identify the color of the person's urine. The identified color is processed with the daily score and the subjective responses to determine hydration.
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
G16H 50/30 - ICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for calculating health indicesICT specially adapted for medical diagnosis, medical simulation or medical data miningICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for individual health risk assessment
A61B 5/0295 - Measuring blood flow using plethysmography, i.e. measuring the variations in the volume of a body part as modified by the circulation of blood therethrough, e.g. impedance plethysmography
57.
Method and system for removing exudates from a wound site
An apparatus (10) for controlling flow of fluid from a wound site of a patient including a cavity (28) connectable to a wound site and a reservoir (16). The cavity (28) may have a first deformed state, and a second state in which it is not deformed or less deformed than in the first state. The cavity (28) may be adapted to manage fluid flow between the wound site and the reservoir (16) during transition of the cavity (28) between the first state and the second state. An actuator element (64) of the apparatus (10) may be adapted to operate on the chamber (28) to transition the cavity (28) from the second state to the first state.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 27/00 - Drainage appliances for wounds, or the like
58.
NEGATIVE PRESSURE WOUND DRESSING MANAGEMENT SYSTEM
A wound exudate management system includes a pump for generating negative pressure, a dressing for covering and protecting a wound of a user, a tube including an interior lumen, the tube disposed between the pump and the dressing such that the pump and the dressing are in fluid communication via the interior lumen. The dressing includes an adhesive layer for adhering the dressing adjacent the wound, a wound contact layer, a pressure dispersion layer, a plurality of layers of absorbent material disposed between the wound contact layer and the pressure dispersion layer, a backing layer having a first surface and a second surface, the first surface of the backing layer being adjacent, and in contact with, the pressure dispersion layer and the adhesive layer, and a flexible connector disposed on the second surface of the backing layer.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A method for determining the hydration status of a person prompts the person to breathe while in a first postural position during which the method measures a first heart rate variability (HRV) value. The person is prompted to change to a second postural position, and the method measures a second HRV value. A difference between the first HRV value and the second HRV value is a daily score. The daily score is subtracted from a baseline to obtain a hydration score. In certain embodiments, the person is requested to respond to a plurality of subjective questions. The method processes the subjective responses and the daily score to determine whether the person is adequately hydrated. In certain embodiments of the method, the person is requested to identify the color of the person's urine. The identified color is processed with the daily score and the subjective responses to determine hydration.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex layer coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
61.
OSTOMY WAFERS INCORPORATING ADHESIVES, OSTOMY DEVICES INCLUDING THE SAME, AND METHODS OF APPLYING
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex surface coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex surface coupled to the external layer.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a foam layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a foam layer coupled to the external layer.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex layer coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
64.
OSTOMY WAFERS INCORPORATING ADHESIVES, OSTOMY DEVICES INCLUDING THE SAME, AND METHODS OF APPLYING
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex surface coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex surface coupled to the external layer.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a foam layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a foam layer coupled to the external layer.
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex surface coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex surface coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
67.
Ostomy wafers incorporating adhesives and foam layers, ostomy devices including the same, and methods of applying ostomy wafers and ostomy devices
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a foam layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a foam layer coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
68.
Perforated chamber ostomy wafers, ostomy devices including the same, and methods of applying ostomy wafers and ostomy devices
Ostomy wafers, ostomy devices incorporating ostomy wafers, and methods of applying ostomy wafers and ostomy devices are disclosed herein. An ostomy wafer may include an external layer and a convex layer coupled to the external layer. An ostomy device may include an ostomy pouch and an ostomy wafer coupled to the ostomy pouch that includes an external layer and a convex layer coupled to the external layer.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
Polymeric superporous hydrogels, methods for making the same, and wound dressings incorporating the same are disclosed herein. The polymeric superporous hydrogels may be PVA-based hydrogel foams. The polymeric superporous hydrogels may exhibit intrinsic antimicrobial activity against Gram-positive bacteria. The polymeric superporous hydrogels may be well suited for incorporation into wound dressings or the like.
A61L 15/60 - Liquid-swellable gel-forming materials, e.g. super-absorbents
A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
A61K 47/34 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
A61L 15/42 - Use of materials characterised by their function or physical properties
70.
SUPERPOROUS HYDROGELS, METHODS OF MAKING THE SAME, AND ARTICLES INCORPORATING THE SAME
Polymeric superporous hydrogels, methods for making the same, and wound dressings incorporating the same are disclosed herein. The polymeric superporous hydrogels may be PVA-based hydrogel foams. The polymeric superporous hydrogels may exhibit intrinsic antimicrobial activity against Gram-positive bacteria. The polymeric superporous hydrogels may be well suited for incorporation into wound dressings or the like.
A61L 15/60 - Liquid-swellable gel-forming materials, e.g. super-absorbents
A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
A61K 47/34 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
A61L 15/42 - Use of materials characterised by their function or physical properties
A wound dressing including a layer in the form of a strip and including gel-forming fibers, the strip having longitudinal lines of stitches formed from a thread and transverse lines of stitches formed from a thread. In certain forms, the wound dressing includes at least one stitch free column.
A chemically modified cellulosic fibre or filament having a moisture content of at least 7% by weight obtained by a process comprising the steps of (i) obtaining cellulosic fibres or filament and chemically modifying the cellulose by substitution to increase its absorbency; (ii) washing the fibres after step (i) in a mixture comprising water and up to 99% by weight of water-miscible organic solvent; (iii) drying the fibres to a moisture content of at least 7% by weight.
D01G 15/00 - Carding machines or accessoriesCard clothingBurr-crushing or removing arrangements associated with carding or other preliminary-treatment machines
B65B 55/02 - Sterilising, e.g. of complete packages
D04H 1/46 - Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
D06M 13/278 - Vinylsulfonium compoundsVinylsulfone or vinylsulfoxide compounds
A61L 15/42 - Use of materials characterised by their function or physical properties
D06M 13/21 - Halogenated carboxylic acidsAnhydrides, halides or salts thereof
D06M 11/38 - Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
A stand-alone system for assessing wound exudates from the wound of a patient is described. The system contains functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may also compare detected physiological values to predetermined physiological values, in order to obtain a comparison result in real time. The system may include a processor (15) which provides an electronic signal based on the comparison result in which the electronic signal may corresponds to guidelines for treating the wound (3). The system described may be an accessory, which may be used on its own, or in conjunction with other wound treatment devices (9).
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using optical sensors, e.g. spectral photometrical oximeters
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
Certain embodiments of the present application relate to an adjustable ostomy wafer system including an ostomy wafer and an insert ring 100. The ostomy wafer includes an adjustable layer with an effluent opening through which effluent flows, and the adjustable layer has a body-facing side and a non-body-facing side. The insert ring 100 is capable of providing or increasing convexity of the adjustable layer when the insert ring 100 is pressed against the non-body-facing side of the adjustable layer.
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
The present invention is a drainable ostomy pouch having a closure system that includes a resealable press and seal material. The material facilitates closing and opening of the ostomy pouch outlet. A space between the comfort panel and the pouch material can accommodate the closure system or at least a portion of the closure system.
A bag connector system includes a first coupling element, with a self-closing seal and a housing having a fluid inlet port and a fluid outlet port, and a second coupling element, with a housing having a fluid inlet end and a fluid outlet end. The fluid inlet end is configured to displace the self-closing seal when inserted into the fluid outlet port of the first coupling element. A bag connector system optionally includes a locking mechanism to maintain the first coupling element and second coupling element in a coupled state. Uncoupling of the first and second coupling elements results in minimal fluid contamination on the outer surfaces of the coupling elements. The bag connector systems provided herein are included in medical appliances for waste management.
F16L 37/38 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in only one of two pipe-end fittings
F16L 37/32 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in each of two pipe-end fittings at least one of two lift valves being opened automatically when the coupling is applied
A61M 39/26 - Valves closing automatically on disconnecting the line and opening on reconnection thereof
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
F16L 37/46 - Couplings of the quick-acting type with fluid cut-off means with fluid cut-off means in only one of two pipe-end fittings with a gate valve or sliding valve
A61F 13/539 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators characterised by the absorbing medium characterised by the connection of absorbent layers with each other or with the outer layers
A61L 15/60 - Liquid-swellable gel-forming materials, e.g. super-absorbents
A61L 15/42 - Use of materials characterised by their function or physical properties
A61F 13/15 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators
A61M 35/00 - Devices for applying media, e.g. remedies, on the human body
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
A rectal drainage appliance is disclosed comprising a tubular element having an inflatable balloon at a distal end for anchoring the appliance in the rectum. The appliance includes one or more of: (i) first and second auxiliary lumens communicating with the inflatable balloon to provide independent inflation and pressure monitoring paths coupled to the balloon; (ii) a pressure state indicator defined by a mechanical element configured to flip between first and second states or shapes responsive to sensed pressure; and (iii) a collapsible auxiliary lumen larger than the inflation lumen, and configured to permit admission of irrigation fluid. The pressure state indicator may also be used in intestinal drains.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 25/04 - Holding devices, e.g. on the body in the body, e.g. expansible
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
A61F 13/42 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators with wetness indicator or alarm
A fluid collection apparatus for use in negative pressure wound therapy. The fluid collection apparatus includes a flexible bag having a first opening and a second opening. The bag includes a structure defining a fluid pathway connecting the first opening and the second opening. The pathway is circulative and contributes to orientation independence of the bag in use. The bag further includes a load-bearing component.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
An ostomy appliance including an ostomy pouch with a filter and a center pleated panel to protect the filter, facilitate deodorization and deter ballooning.
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
A staining composition for use in making biofilm detectable on viable tissue wherein the composition preferentially stains the biofilm and comprises a staining agent in a quantity effective to stain the biofilm and render it detectable.
G01N 33/569 - ImmunoassayBiospecific binding assayMaterials therefor for microorganisms, e.g. protozoa, bacteria, viruses
C12Q 1/04 - Determining presence or kind of microorganismUse of selective media for testing antibiotics or bacteriocidesCompositions containing a chemical indicator therefor
G01N 33/533 - Production of labelled immunochemicals with fluorescent label
G01N 33/58 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving labelled substances
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 27/00 - Drainage appliances for wounds, or the like
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61M 27/00 - Drainage appliances for wounds, or the like
90.
High barrier elastomer fecal catheter or ostomy pouch
A fecal catheter or ostomy pouch made of an odor barrier material including a thermoplastic elastomer, odor barrier modifier and an antiblocking agent.
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value using optical sensors, e.g. spectral photometrical oximeters
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value
93.
Negative pressure wound dressing management system
A wound exudate management system includes a pump for generating negative pressure, a dressing for covering and protecting a wound of a user, a tube including an interior lumen, the tube disposed between the pump and the dressing such that the pump and the dressing are in fluid communication via the interior lumen. The dressing includes an adhesive layer for adhering the dressing adjacent the wound, a wound contact layer, a pressure dispersion layer, a plurality of layers of absorbent material disposed between the wound contact layer and the pressure dispersion layer, a backing layer having a first surface and a second surface, the first surface of the backing layer being adjacent, and in contact with, the pressure dispersion layer and the adhesive layer, and a flexible connector disposed on the second surface of the backing layer.
A61M 1/00 - Suction or pumping devices for medical purposesDevices for carrying-off, for treatment of, or for carrying-over, body-liquidsDrainage systems
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
A61F 13/42 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators with wetness indicator or alarm
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
G01K 3/10 - Thermometers giving results other than momentary value of temperature giving differences of valuesThermometers giving results other than momentary value of temperature giving differentiated values in respect of time, e.g. reacting only to a quick change of temperature
An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
A61F 5/44 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61F 5/441 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having deodorant means, e.g. filters
G01F 23/26 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
G01K 13/02 - Thermometers specially adapted for specific purposes for measuring temperature of moving fluids or granular materials capable of flow
A61F 13/42 - Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the bodySupporting or fastening means thereforTampon applicators with wetness indicator or alarm
A stoma adapter is described that is especially suited to a recessed stoma or a flush stoma. The stoma adapter effectively extends the discharge passage from the stoma, protects peristomal skin, and forms a bridge at the interface between the stoma and an ostomy appliance. The stoma adapter contains a substantially unobstructed discharge passage, at least for effluent flowing in a discharge direction. The stoma adapter includes a seal for sealing against the bowel wall. The stoma adapter has collapsing, expanding, flexible and reinforced designs.
A wound dressing including a nonwoven absorbent layer including a layer of fabric comprising gel-forming fibers. The absorbent layer is gathered in a longitudinal direction by stitching through the layer of fabric using one or more resilient threads or yarns and an inelastic thread or yarn. The resilient and inelastic threads or yarns gather the layer of fabric so that the layer of fabric in use is configured to maintain close conformability with a wound during movement, and to elongate by 35% to 85% and then recover.
A silicone pressure sensitive adhesive with amphiphilic copolymers for maintaining adhesion in a moist environment. The amphiphilic copolymers for silicone adhesives include at least one silicone moiety and at least one hydrophilic segment. Such adhesives are applicable to securing medical devices to human skin.
C08F 230/08 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
C08L 83/00 - Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon onlyCompositions of derivatives of such polymers
C08G 77/00 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon
C09J 7/30 - Adhesives in the form of films or foils characterised by the adhesive composition
C09J 183/00 - Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon onlyAdhesives based on derivatives of such polymers
C09J 143/04 - Homopolymers or copolymers of monomers containing silicon
C08G 77/20 - Polysiloxanes containing silicon bound to unsaturated aliphatic groups
C09J 183/14 - Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon onlyAdhesives based on derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
A coupling assembly for fastening an adhesive wafer to an ostomy appliance device, the coupling assembly including a captive connection between the adhesive wafer and ostomy appliance that permits captive relative displacement between the entire adhesive wafer and the entrance aperture of the appliance, to facilitate access to the wafer from the non-body-contacting side. The coupling assembly further comprises a fixation coupling for fixing the adhesive wafer in the operative position.
A61F 5/443 - Devices worn by the patient for reception of urine, faeces, catamenial or other dischargeColostomy devices having hydrocolloid type seals, e.g. gels, starches, karaya gums
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