Abstract: An improved injection port identification for injection ports implanted under the skin of a patient. The injection port has an x-ray discernable marker allowing for the determination of a pressure rating for the injection port when so implanted. A plurality of concurrent visual, RF, light emitting and sonic means for signaling the port's pressure rating are also employable to provide multiple concurrent affirmations of the port's readiness for high pressure injections.

Abstract: The wound protector has an annularly collapsible proximal ring and a flexible sleeve extends between the proximal ring and distal ring. After positioning of the distal ring in a wound, the proximal ring is expanded to draw the sleeve taut between the rings and is drawn tight against the wound. In one embodiment, the proximal ring includes a bent hollow tube with an arcuate rod in the tube bridging the open ends of the tube and a compression spring extending within the tube against the ends of the rod to bias the proximal ring into an extended state. Finger grips on the ends of the tube allow for squeezing of the tube into a collapsed state.

Abstract: In one embodiment, the dressing has a base which is to be adhered to a patient about a catheter site, an aperture in the base to pull a catheter line through and a cover with a window that is folded over and onto the base in a sealed manner. In another embodiment, the dressing has two covers with windows for folding over separate sections of a base to seal in the components of a catheter assembly with multiple catheters extending from a common housing.

Abstract: In one embodiment, the dressing has a base which is to be adhered to a patient about a catheter site, an aperture in the base to pull a catheter line through and a cover with a window that is folded over and onto the base in a sealed manner. In another embodiment, the dressing has two covers with windows for folding over separate sections of a base to seal in the components of a catheter assembly with multiple catheters extending from a common housing.

Abstract: An improved injection port identification for injection ports implanted under the skin of a patient. The injection port has an x-ray discernable marker allowing for the determination of a pressure rating for the injection port when so implanted. A plurality of concurrent visual, RF, light emitting and sonic means for signaling the port's pressure rating are also employable to provide multiple concurrent affirmations of the port's readiness for high pressure injections.

Abstract: The dressing has a first section that includes a bubble for covering over a housing of a Huber needle embedded in a patient and a second section that folds over the first section to encase a tubing of the Huber needle between the two sections. A slit is formed in the first section to allow passage of the tubing. In one embodiment, an insert of foam material is provided in the bubble to rigidify the bubble.

Abstract: A fluid drainage system is provided which is configured to engage with a drainage tube engaged with a drainage site with a patient. The container has an internal cavity with negative pressure to impart suction to the drainage tube and can be engaged to the drainage tube without loss of negative pressure during the process. Secondary containers may be engaged to restore negative pressure to the first container and remove fluid therefrom. Walls of the first container may be shaped to resist deflection due to high internal negative pressure.

Abstract: A microcatheter deliverable implant is provided formed of an elongated wire of a diameter capable of delivery through the axial passage of such a microcatheter. A first portion of the formed implant forms a coiled first section larger in diameter than an anomaly to be blocked. A second portion formed by the coiled wire engages the implant between the first and second portions to block communication of fluid through the anomaly.

Abstract: A device for the drainage of a pleural effusion through an operatively engaged chest tube in the chest wall. The device employs a check valve situated between a vacuum source communicating with the chest tube to prevent reversal of the fluid flow out of the patient's body and possible contamination. A valve mounted on a vacuum bottle provides user control of communication of negative pressure from the vacuum bottle to the chest tube. Opening the valve on the bottle communicates negative pressure to the chest tube relative to the pressure in the tube thereby initiating a fluid flow out of the tube and the patient. Once the valve on the bottle is closed, fluid flow ceases and the check valve prevents reversal of the flow.

Abstract: The wound protector has an annularly collapsible distal ring, an expansion member and a flexible sleeve extending between the distal ring and expansion member. After positioning of the distal ring in a wound, movement of the expansion member into an extended state expands the sleeve while drawing the sleeve tight against the wound and the expansion member against the patient.

Abstract: The dressing has a pad for adhesive securement to a patient that includes a bubble for covering over a housing of a Huber needle assembly embedded in the patient. A slit is formed in the pad to allow passage of the tubing of the Huber needle assembly. In one embodiment, an insert of foam material is provided in the bubble to rigidify the bubble. A second section may also be provided for folding over the pad to encase the tubing, catheter and clamp of the Huber needle assembly.

Abstract: An improved injection port for implantation within a patient having an x-ray discernable marker allowing for the determination of a pressure rating for the injection port when so implanted.

Abstract: In one embodiment, the dressing has a base which is to be adhered to a patient about a catheter site, an aperture in the base to pull a catheter line through and a cover with a window that is folded over and onto the base in a sealed manner. In another embodiment, the dressing has two covers with windows for folding over separate sections of a base to seal in the components of a catheter assembly with multiple catheters extending from a common housing.

Abstract: A one-piece connector for removing a housing and needle of a Huber needle assembly from a patient. The connector has a frame that can be positioned about a surface on the housing of the needle assembly and a pair of wings that pivot toward one another to provide a gripping surface.

Abstract: A mesh device for supporting one or a combination of a breast implant or breast tissue is provided formed of interlaced filaments forming a mesh structure which will not unravel when cut across a mid section of the mesh device. A titanium layer positioned on the exterior surface of the filaments of the mesh provide both a biocompatible interface with surrounding tissue and enhanced engagement of the filaments to prevent unraveling.

Abstract: The wound protector has an annularly collapsible proximal ring and a flexible sleeve extends between the proximal ring and distal ring. After positioning of the distal ring in a wound, the proximal ring is expanded to draw the sleeve taut between the rings and is drawn tight against the wound. In one embodiment, the proximal ring includes a bent hollow tube with an arcuate rod in the tube bridging the open ends of the tube and a compression spring extending within the tube against the ends of the rod to bias the proximal ring into an extended state. Finger grips on the ends of the tube allow for squeezing of the tube into a collapsed state.

Abstract: A bio-compatible lumen bearing device such as a catheter formed of a polymeric material having a titanium surface bonded to the underlying exposed catheter surface. The titanium surface is employed in patients to improve bio-compatibility and enhance lubricity during insertion and removal.

Abstract: In one embodiment, the wound protector has an annularly collapsible proximal ring and a flexible sleeve extends between the proximal ring and distal ring. After positioning of the distal ring in a wound, the proximal ring is expanded to draw the sleeve taut between the rings 11, 12 and is drawn tight against the wound. In a second embodiment, the wound protector has a flexible sleeve secured between a distal ring and proximal ring of fixed diameters. In addition, an expansion member is disposed within a loop of the flexible sleeve about the proximal ring. After positioning of the distal ring in a wound, movement of the expansion member into an extended diametric state expands the loop in the sleeve diametrically while drawing the rings towards each other.