Abstract: By providing a non-liquid drug reservoir layer 2 having first and second principal surfaces and containing a drug and a polymer that is to be a base, a drug permeation layer 4 disposed at the first principal surface side of the drug reservoir layer 2 and being lower in permeability of the drug than the drug reservoir layer 2, and a first backing 3 with a bending resistance of 10 to 80 mm that is formed so as to cover a side surface of the drug reservoir layer, skin irritation can be reduced.

Abstract: A sanitary protection device intended to be placed in the user's vagina (7). Distinguishing features of the sanitary protection device are that it includes a shell-like basic element (1), that the basic element (1) has in its height direction (H) a shape which narrows both upwards and downwards from an intermediate portion, and that the basic element (1) is provided with apertures (5) along part of its external surface.

Abstract: A system for transferring solutions from a first cartridge into a second cartridge comprises a cartridge holder, a plunger driver, and a cartridge connector. The cartridge connector carries a transfer needle and an exhaust needle. The cartridge holder positions the first cartridge against the cartridge connector so that the transfer needle penetrates the first cartridge septum. The second cartridge is removably inserted into another end of the cartridge connector so that both the transfer needle and the exhaust needle penetrate the second cartridge septum. The plunger driver is disposed to advance a plunger on the first cartridge to transfer solution from the first cartridge into the second cartridge thus displacing solution from the second cartridge through the exhaust needle. The cartridge connector includes a sealed interior waste chamber for receiving the solution from the second cartridge.

Abstract: An improved wound care system is set forth. The system includes a wound care device having a first end and a second end. A fastener, adapted to extend to a desired length to selectively attach the device at an anchor, wherein the anchor is provided on a second end of the device is also provided. The fastener is sufficiently sized and formed of a suitable material to prevent the device from moving when secured to the anchor. In an embodiment, medicine is provided in a desired treatment area of the device. The medicine can be inserted via a medicinal delivery device by inserting the medicinal delivery device up to a stop on the medicinal delivery device into the wound care device.

Abstract: A controlled evacuation ostomy appliance comprises a pouch having a non-entrant stoma seal and a retainer for retaining the lower portion of the pouch in the folded-up condition. The appliance optionally includes a body fitment that may include a region of manually moldable adhesive for forming a custom fit at the stoma.

Abstract: A device for the flow rate limitation at low differential pressures, in particular for the limitation of the inhalation volume flow during the inhalation of therapeutic aerosols, comprising a housing with at least an inlet opening, at least an outlet opening and a flow channel arranged therebetween, wherein the flow channel is restricted by a flexible wall extending along the flow channel, characterized in that the flexible wall has a control area of less than 100 mm2.

Abstract: A system for delivering moisturizing liquid to the lips of a subject includes an applicator for applying the moisturizing liquid to the lips supported by a support structure so that at least a part of applicator is deployed so as to engage a recess between the lips of subject without obstructing contact between the subject's upper and lower lips. The proximity of the applicator to the lips allows the use of simple contact-based implementations of the applicator. At the same time, disruption of speech and other normal oral movement is minimized by avoiding any obstruction to contact between the lips.

Abstract: Radially divided adhesive wafers are provided for applying to the skins of a human, and which increase the wear time for such adhesive wafers. The adhesive wafer includes a through-going hole for communication with a body opening and an adhesive proximal side for attachment of the wafer to the skin. The adhesive wafer has an inner annular adhesive layer, an outer annular adhesive layer encircling the inner annular adhesive layer, an attachment zone on the distal side of the wafer for attaching a collection bag, and a connecting element for mechanically connecting the first annular adhesive layer to the second annular adhesive layer. The connecting element includes first and second connection areas on the distal side of the respective first and second annular adhesive layers, at least one connection area being radially spaced from the radial edges of the respective annular adhesive layer.

Abstract: A convex barrier ring, that includes a generally oval shaped body and tapered peripheral end portions, is provided. In use, the convex barrier ring is sealed against peristomal skin surfaces such that the tapered peripheral end portions are aligned with folds or creases in the skin surfaces to reduce leakage of stomal effluent. The convex barrier can also have an oval stoma-receiving aperture to provide an improved fit for oval or loop stomas.

Abstract: A body waste collecting device comprising a collecting pouch and an adhesive wafer for attachment to the body, said adhesive wafer comprises a backing layer, a first adhesive and an additional second adhesive, wherein said additional second adhesive comprises a polar plasticizing oil or a combination of polar plasticizing oils in the content of above 10% (w/w) of the final second adhesive, and at least one polar polyethylene copolymer, wherein the content of the polyethylene copolymer is 10-50% (w/w) of the final second adhesive, the polyethylene copolymer has a melt flow index below 2 g/10 min (190° C./21.1 N).

Abstract: An intubating attachment apparatus for use with endotracheal intubation devices comprising an elongated, generally cylindrical support module configured to accommodate a fiber optic intubation scope and at least one of an endotracheal tube or an endotracheal tube exchanger. The invention obviates the need for an attending medical professional to utilize more than one hand when advancing an endotracheal tube and/or endotracheal tube exchanger along with the fiber optic bundle of a bronchoscope into a patient.

Abstract: A discharging device, particularly for a pharmaceutical liquid, is adapted to accommodate and actuate a pump-type dispenser in an accommodating region. In the delivered state, the accommodating region of the discharging device is sufficiently large to ensure that the pump-type dispenser can be accommodated by the accommodating region when the dispenser has not yet been actuated and does not yet communicate with the outlet passageway. The discharging device is particularly useful for pharmaceutical liquids prone to oxidation and thus in need of extensive protection from contact with air.

Abstract: A method is described comprising: providing a first heated volume flow of pressurized gas, a second volume flow of pre-heated dilution gas, and a third volume flow of fluid. A concentrated first aerosol is generated by exhausting at least a part of the first volume flow of pressurized gas and the third volume flow of fluid through a nozzle. A fourth volume flow of gas of opposite direction to the concentrated first aerosol is generated such that the concentrated first aerosol is arrested. Evaporation of the aerosol solvent is augmented with infrared radiation. The arrested first aerosol is then mixed with the second volume flow of dilution gas for generating a second aerosol that has been diluted. This aerosol is then concentrated with a virtual impactor.

Abstract: Methods and apparatus for treatment of dry eyes by providing a single apparatus for measuring the diameter of the lacrimal punctum and, based on the measured punctal diameter, inserting therein an appropriately sized punctum plug.

Abstract: A fluid extraction or filtration device for removing fluid from a body, the device comprising an array of microneedles for contacting fluid in said body and an absorbent gel matrix in fluid communication with said array of microneedles. There is further provided a combined fluid extraction and sampling device and methods employing the device(s), for example in determining the level of a target species in a sample of fluid, transdermal dialysis and renal replacement therapy. There is further provided an absorbent gel matrix for use in the treatment of uraemia and a haemodialysis filter comprising an absorbent gel matrix. Use of such a matrix is described in the context of methods including haemodialysis, transdermal dialysis and gastrointestinal dialysis.

Abstract: A dispensing device and a storage device for dispensing a formulation as a spray. The storage device has multiple separate and pre-metered doses of the formulation in receptacles or cavities. In order to allow a very compact arrangement, the receptacles or cavities are arranged in a first group and a second group axially offset, and preferably, forming a double ring arrangement, and the storage device is rotatable and axially moveable for dispensing the doses one after the other.

Abstract: An assembly for modifying airflow into a nasopharyngeal airway or trachea of a patient. A valve assembly having an inlet and an outlet attaches to a traditional airflow generator. A valve seal within the assembly is operable by a solenoid and is adapted to cycle in response to a programmable controller circuit wherein upon activation of both the airflow generator and the controller circuit, pressurized air from the airflow generator continuously enters the inlet but passes out of the outlet of the assembly only when the solenoid causes the valve seal to retract and to at least partially unblock the outlet such that the pressurized air is converted into a single, repeatable burst exiting the outlet thereby modifying the traditional airflow.

Abstract: A suction apparatus evacuates the surgical smoke. For example, the suction apparatus may be arranged adjacent to an electrocautery electrode, which may generate smoke during operation, for evacuating smoke from a surgical site. The suction apparatus may include replaceable suction tips that correspond in shape to differently shaped electrocautery electrodes.

Abstract: A connector is configured to be connected to a syringe assembly provided with at least one syringe having an outer cylinder with a protruding tube-shaped port, and a holder which holds the syringe. The connector includes a connector main body mountable on a container containing a medical solution; a tube-shaped fitting section protruding from the upper section of the connector main body for receiving the syringe to connect the inside of the syringe and the inside of the container when the syringe port is fitted in the fitting section; and fixing means having a lock mechanism that fixes the syringe assembly to the connector main body when the syringe port is fitted in the fitting section, an operating section to release the fixed state provided by the lock mechanism, and a push-out section that pushes out the syringe assembly when the fixing releasing operation is performed.

Abstract: A solid stepped needle delivers a disc shunt bridging between muscle and a degenerated disc, drawing blood plasma from muscle into the degenerated disc to alleviate back pain and regenerate the disc. The device further includes pull lines attached to the ends of the disc shunt for withdrawing and repositioning the stepped needle during shunt delivery.