Abstract: An infusion apparatus containing a medicament and volume of diluent for reconstituting the medicament and dispensing in an infusion therapy in a controlled and measured amount.

Abstract: A method for processing biological material containing stringy tissue in a container having a tissue collector disposed in a tissue retention volume on one side of an internal filter includes washing biological material contained in the tissue retention volume with wash liquid to the tissue retention volume and allowing the wash liquid and rotating the tissue collector disposed in the tissue retention volume relative to the container in a first direction of rotation about an axis of rotation to sweep the teeth positioned on the tissue collector through the biological material and to collect stringy material on the tissue collector.

Abstract: An apparatus is disclosed. The apparatus includes a catheter guide (10, 10?, 10?, 10??, 10??). The catheter guide (10, 10?, 10?, 10??, 10??) includes a first conduit (12, 12?, 12?, 12?? 12??) a second conduit (14 14? 14? 14?? 14??) and a shield member (16 16? 16?, 16??, 16??). The second conduit (14, 14?, 14?, 14??, 14??) is connected to an outer surface (26, 26?, 26?, 26??, 26??) of the first conduit (12, 12?, 12?, 12??, 12??).

Abstract: Systems, methods, and dressing are presented for treating a tunnel wound on a patient. In one instance, a reduced-pressure, tunnel-wound dressing includes a longitudinal core member formed from a closed-cell foam that is surrounded by a first longitudinal concentric member formed from a manifolding material. When subjected to reduced pressure, the longitudinal core member expands and the first longitudinal concentric member compresses. These actions create intimate contact between the tunnel wound and the dressing, oppose collapse of the tunnel, and when reduced pressure is removed provide clearance to remove the dressing. Other embodiments are presented.

Abstract: An apparatus for extracorporeal blood treatment comprises a sensor (10) for emitting a signal indicating a variation in blood volume (?Bv?) of an individual (7) subjected to extracorporeal blood treatment and a sensor (14) for emitting a signal indicating a weight loss of the individual. A control unit (20) receives the signals, compares the ratio between the relative variation of blood volume (?Bv/BV) and the relative variation of weight loss (AWL/TW) of the individual with a desired value, and controls the weight loss of the individual on the basis of the comparison. The apparatus enables automatically controlling a dialysis, preventing some complications due to hypotension.

Abstract: The invention relates to a medical device for extracorporeal blood treatment comprising an extracorporeal blood circulation having at least one tube and at least two sensor units measuring on the tube with different operating principles, wherein portions of the tube are adapted to be coupled to the at least two sensor units for measurement. According to the invention, each sensor unit consists of a sensor-specific component and a sensor-neutral component, wherein the sensor-neutral components of the sensor units are formed to be identical whereas the sensor-specific components are different in response to the operating principle and comprise a respective specific sensor system.

Abstract: Provided are systems, dressings, and methods suitable for treating a tissue site, such as an incision or linear wound. The systems, dressings, and methods relate to a dressing assembly that may include a dressing bolster and a sealing ring. The sealing ring may be adapted to provide a fluid seal around the tissue site, and to absorb fluids from the tissue site. In some embodiments, the sealing ring may be extruded around the tissue site. In other embodiments, the sealing ring may be coupled to the dressing bolster. Other systems, apparatuses, and methods are disclosed.

Abstract: Systems, methods, and apparatuses for providing feedback for reduced-pressure treatment of a tissue site are described. A regulator may include a supply chamber fluidly coupled to the dressing, a control chamber fluidly coupled to the dressing, a charging chamber fluidly coupled to the supply chamber through a port, and a regulator valve operable to control fluid communication through the port based on a pressure differential between the control chamber and a therapy pressure. The feedback system may include one or more mechanical feedback interfaces fluidly coupled to the regulator to provide a signal of at least one of an application of reduced-pressure therapy, a leak condition, a blockage condition, and a canister full condition.

Abstract: A waste collection system for collecting waste during medical/surgical procedures including a mobile container cart with a waste container. A container cart is selectively coupled to a suction cart that includes a vacuum pump. The connection of the carts results in the connection of the vacuum pump to the waste container. The vacuum pump draws a vacuum that results in waste being drawn through a suction line into the waste container. The container cart holds instruments that can be removably attached to the container cart. This facilitates the configuration of the container cart for the specific procedure for which it is necessary to draw a suction.

Abstract: A multi-lumen catheter, for insertion into and draining a body cavity, that mitigates the risk of obstruction of the drainage ports and drainage lumen of the catheter, reduces the detrimental effects caused by the suction forces of the drainage ports on the body cavity being drained, and reduces the risk of infection of the body cavity being drained by decreasing the residual volume of fluid retained in the body cavity being drained. These advantages are achieved by the novel approach of disposing a perforated filter membrane or a membrane having a relatively large entry port(s) between membrane struts over a segmented retention element and also over the drainage port(s) of the drainage lumen of the catheter thereby creating internal interstitial drainage channels and internal interstitial drainage cavities.

Abstract: A device (1) for the application of liquid medical substances (100) comprises a main body (2) extending around a longitudinal axis (X) and comprising a housing portion (3) at a first open end (4) and a delivery portion (5) at a second open end (6) which is opposite the first (4); a hermetically sealed cartridge reservoir (7) containing a liquid medical substance (100); a perforating element (8) disposed inside the main body (2) in a position falling between the housing portion (3) and the delivery portion (5) and such as to achieve the perforation of one end of the cartridge reservoir (7). The perforating element (8) has a tubular shape and comprises, in a central portion thereof, a cylindrical conduit (12) having a cutting edge (14) faced towards the housing portion (3).

Abstract: A multi-lumen catheter, for insertion into and draining a body cavity, that mitigates the risk of obstruction of the drainage ports and drainage lumen of the catheter, reduces the detrimental effects caused by the suction forces of the drainage ports on the body cavity being drained, and reduces the risk of infection of the body cavity being drained by decreasing the residual volume of fluid retained in the body cavity being drained. These advantages are achieved by the novel approach of disposing a perforated filter membrane over a segmented retention element and also over the drainage ports of the drainage lumen of the catheter thereby creating internal interstitial drainage channels and internal interstitial drainage cavities.

Abstract: A two phase method for reducing the formation of biofilm includes an evacuation of ambient air from a region about the surgical or treatment site, to extract airborne or aerosolized bacteria ejected from the site by the treatment. The extracted bacteria are prevented from settling back onto the cleansed tissue surface, thus at least reducing colonial bacteriological growth and concomitantly exuded biofilm material. A second phase involves the attachment of one or more ultrasonic transducers to the patient over or near a surgical treatment site after the surgery is terminated. Each applied ultrasonic transducer is used to vibrate the patient's tissues at the treatment site to disrupt biofilm formation.

Abstract: The present invention relates to a device that secures a straight or Foley catheter in the urinary tract of a male subject. The device includes a portion that can be coupled to the subject's penis and a portion that can be coupled to the straight or Foley catheter. The present invention also relates to methods of making and using this device and to assemblies including the device and a straight or Foley catheter.

Abstract: A prosthesis (14) that is useful as an anti-reflux device or an anti-obesity device within a gastro-intestinal tract of a living organism, such as a human, comprises an elastic portion including a helical elastic spring (15) embedded in a biocompatible material.

Abstract: An implantable prosthesis is provided for repairing a fistula, such as an anal fistula. The prosthesis or fistula repair device may include a body with a shape configured for placement in the fistula. The prosthesis may also include an anchor or base that is located at one or both ends of the body to facilitate anchoring the prosthesis in position. The prosthesis may include one or more channels to create one or more pathways for drainage and/or irrigation of the fistula. The channel may have a relatively uniform dimension along its length or a tapered shape that increases along its length. The prosthesis may have an adjustable length for accommodating fistula tracts of varying lengths. The prosthesis may include elongated body segments that provide a wicking or capillary function to facilitate drainage of the fistula tract.

Abstract: A dry peritoneal dialysis (PD) concentrate system may be used in connection with a PD cycler. The dry PD concentrate system includes a concentrate container with at least two concentrate compartments, and at least one of the compartments contains a dry PD concentrate component. At least one of the concentrate compartments has a medical fluid outlet, and at least one of the concentrate compartments has a diluent inlet.

Abstract: Systems, methods, and kits useful for cleansing the eyelids and maintaining eyelid hygiene are disclosed. In one embodiment, a system for treating or cleansing an ocular region is disclosed. The system consists essentially of: (A) a tubular applicator, wherein the applicator comprises: (i) a first chamber and a second chamber; and (ii) a sealable element situated between the first chamber and the second chamber, wherein at least the second chamber is substantially pre-filled with an ocular composition, and (B) a dispenser, wherein the dispenser is bonded to an external surface of a first end of the applicator.

Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen and have in a wall a hole for guiding a lacrimal duct tube operative instrument to the lumen; and a connection member that connects the other ends of the tubular members. Surfaces of the tubular members include a hydrophilic-coated portion and a non-coated portion without the hydrophilic coating. It is preferred that the lumen in the vicinity of the opening includes an engagement portion for engagement with a tip of the lacrimal duct tube operative instrument, and the non-coated portion is formed without overlapping with the surface of the tubular member at the position of the engagement portion. The lacrimal duct tube can be used favorably for various lacrimal duct obstruction treatments. In the case of using a sheath such as in sheath guided endoscopic probing, the lacrimal duct tube can be easily inserted into the sheath and be firmly fixed to the sheath.

Abstract: A safety sealed bottle stopper in the form of a one-piece unitized fusion over-molded injection molded component comprising an exterior housing having multiple sealing fins forming an internal liquid leakproof engagement with the interior bottle neck of a liquid medication bottle container and having an upper entrance port and a lower fluid flow path with a valve positioned between the lower fluid communication path and the upper entrance port. The upper entrance port is configured to form a liquid tight engagement fit only with an oral/enteric tip syringe and not with an I.V. (intravenous) luer slip tip syringe to indicate to the user that the stopper is only to be used with an oral/enteric syringe and not an I.V. luer slip tip syringe as a safety feature which is especially useful when the stopper is used as part of an infant's or child's liquid medication bottle container.