Abstract:
A valve for sealing the hub of a sheath assembly is provided. The valve includes a valve body having a solid thickness extending between a proximal surface and a distal surface. A bisecting slot extends across the proximal surface of the valve body and terminates at a depth less than the thickness of the valve body such that a portion of the valve body distally of the slot defines a bridge extending between opposed halves of the valve body such that the distal surface of the valve body is substantially continuous and a central portion of the proximal surface of the valve body is concave and defines a concave proximal portion.
Abstract:
A sealing arrangement for a medical introducer having a distal end for introduction into a patient's blood vessel. The introducer includes a flexible sealing member having an aperture for introduction of a guide wire or other medical device therethrough. A constraining structure, such as a washer, tightly contacts and surrounds the sealing member just proximal to an enlarged diameter flange at the distal end of the sealing member. The inner diameter of the constraining member is less than the outer diameter of the flange providing a constraint on the sealing member and lessening the distortion of the sealing member normally occasioned when a device is pulled outwardly or proximally through the introducer away from the patient. When the constraining structure is a washer, the washer is easily assembled to the introducer by simply being fitted into an annular notch formed just proximal to the distal end of the sealing member.
Abstract:
A hernia repair implant includes a first layer for facing a body structure having a hernia defect to cover the defect while promoting tissue growth into the first layer from the body structure. The implant also includes a second layer opposed to the first layer and made of anti-adhesion material to prevent growth of tissue into the second layer from body structures contacting the second layer. Furthermore, the implant includes at least one engagement strap connected to the first layer and extending therefrom to terminate at a free end. The engagement strap defines opposed thin edges and opposed flat surfaces extending between the edges. At least one barb extends from at least one edge and/or at least one flat surface of the strap and is configured to impede motion of the strap in only a single direction.
Abstract:
A catheter connector and method of use is disclosed. The catheter connector includes a body, a proximal end port, and a seal. The body has a proximal end and a distal end. Further, the body defines a hollow interior from the proximal end to the distal end. The hollow interior is configured to receive a catheter at least partially therethrough. The proximal end port includes a cavity and is configured with the proximal end of the body for mating communication with a fluid delivery device, such as a pump, reservoir, syringe, or the like. This port may have any conventional configuration, such as a Luer-lock fitting. The seal is configured within the interior of the body and includes a passage configured for receipt of the catheter. In addition, at least a portion of the seal is configured within the cavity of the proximal end port. Further, the seal is configured to compress around the catheter so as to axially secure the catheter within the body.
Abstract:
A method includes logically associating an intravenous catheter and an electronic patient record stored on a computer readable storage medium, wherein the electronic patient record includes medical information specific to an identified patient. An identification code of a syringe to be administered to the identified patient is read in order to identify a liquid contained in the syringe. The blocking member may be electronically actuated to provide fluid communication between a catheter chamber and a catheter line inserted into the identified patient, wherein the fluid communication is provided only while the syringe is received within the catheter chamber and only in response to determining that administration of the identified liquid to the identified patient is compatible within the medical information.
Abstract:
A hernia repair implant includes a first layer for facing a body structure having a hernia defect so cover the defect while promoting tissue growth into the first layer from the body structure. The implant also includes a second layer opposed to the first layer and made of anti-adhesion material to prevent growth of tissue into the second layer from body structures contacting the second layer. Furthermore, the implant includes at least one engagement strap connected to the first layer and extending therefrom to terminate at a free end. The engagement strap defines opposed thin edges and opposed flat surfaces extending between the edges. At least one barb extends from at least one edge and/or at least one flat surface of the strap and is configured to impede motion of the strap in only a single direction.
Abstract:
A hernia repair implant includes a first layer for facing a body structure having a hernia defect to cover the defect while promoting tissue growth into the first layer from the body structure. The implant also includes a second layer opposed to the first layer and made of anti-adhesion material to prevent growth of tissue into the second layer from body structures contacting the second layer. Furthermore, the implant includes at least one engagement strap connected to the first layer and extending therefrom to terminate at a free end. The engagement strap defines opposed thin edges and opposed flat surfaces extending between the edges. At least one barb extends from at least one edge and/or at least one flat surface of the strap and is configured to impede motion of the strap in only a single direction.
Abstract:
A hernia repair implant includes a first layer for facing a body structure having a hernia defect to cover the defect while promoting tissue growth into the first layer from the body structure. The implant also includes a second layer opposed to the first layer and made of anti-adhesion material to prevent growth of tissue into the second layer from body structures contacting the second layer. Furthermore, the implant includes at least one engagement strap connected to the first layer and extending therefrom to terminate at a free end. The engagement strap defines opposed thin edges and opposed flat surfaces extending between the edges. At least one barb extends from at least one edge and/or at least one flat surface of the strap and is configured to impede motion of the strap in only a single direction.
Abstract:
A bottomed, tubular hollow elastic body that opens toward an outlet side of a drug solution flow path is accommodated and arranged in an accommodation part formed in a housing, and a middle protrusion is provided protruding toward an inlet side of the drug solution flow path from a center part of a bottom wall of the hollow elastic body. Insertion of a male luer causes the bottom wall of the hollow elastic body to be elastically deformed so as to enter inside a peripheral wall, increasing the volume of the drug solution flow path, which is formed between an outer surface of the hollow elastic body and an inner surface of the accommodation part. Removing the male luer and canceling the elastic deformation of the hollow elastic body causes the volume of the drug solution flow path to be reduced.
Abstract:
Systems and methods to provide an intravenous device having flashback capabilities and features to permit a flashback notch of an introducer needle to bypass a septum of the device without incurring an undesirable contact between the flashback notch of the introducer needle and a related contact surface of the septum.