Abstract: Catheters adapted for use in small body vessels are described. A catheter includes an elongate shaft having a main body that defines first and second lumens. An inner tubular member is disposed in the second lumen and is formed of a material that has a stiffness that is greater than a stiffness of the material forming the main body.

Abstract: Catheters adapted for use in small body vessels are described. A catheter includes an elongate shaft having a main body that defines first and second lumens. An inner tubular member is disposed in the second lumen and is formed of a material that has a stiffness that is greater than a stiffness of the material forming the main body and that has an elastic modulus greater than or equal to about 400 MPa.

Abstract: A sheath for deploying a medical device to a target site in the body of a patient. A tubular inner liner has a proximal portion, a distal portion, and an outer surface. An outer jacket has a proximal portion, a distal portion, and an inner surface. A reinforcing member is received within a length of the outer jacket. The outer jacket is positioned longitudinally around the inner liner and bonded to the outer surface of the liner. The reinforcing member, which may be a triaxial braid, or an encapsulated longitudinal reinforcing wire, extends along the outer jacket length and is configured for inhibiting elongation of the sheath upon deployment of the device.

Abstract: A sheath for deploying a medical device to a target site in the body of a patient. A tubular inner liner has a proximal portion, a distal portion, and an outer surface. An outer jacket has a proximal portion, a distal portion, and an inner surface. A reinforcing member is received within a length of the outer jacket. The outer jacket is positioned longitudinally around the inner liner and bonded to the outer surface of the liner. The reinforcing member, which may be a triaxial braid, or an encapsulated longitudinal reinforcing wire, extends along the outer jacket length and is configured for inhibiting elongation of the sheath upon deployment of the device.

Abstract: A method of forming a reinforced tubular medical device in a continuous operation, and a medical device formed by the continuous method. An elongated core capable of movement about a line is provided. An elongated tubular member is formed around a moving length of the core by extruding a coating of a functionalized polymer around the moving core length, applying a reinforcing member to an outer surface of the functionalized polymer coating along the moving length, and extruding a polymeric outer jacket over the functionalized polymer and reinforcing member along the moving length, such that a bond is formed between the functionalized polymer and the polymeric outer jacket. The elongated tubular member is cut to desired length to form the tubular medical device, and the core is removed from the device.

Abstract: Catheters adapted for use in small body vessels are described. A catheter includes an elongate shaft having a main body that defines first and second lumens. An inner tubular member is disposed in the second lumen and is formed of a material that has a stiffness that is greater than a stiffness of the material forming the main body and that has an elastic modulus greater than or equal to about 400 MPa.

Abstract: A sheath for deploying a medical device to a target site in the body of a patient. A tubular inner liner has a proximal portion, a distal portion, and an outer surface. An outer jacket has a proximal portion, a distal portion, and an inner surface. A reinforcing member is received within a length of the outer jacket. The outer jacket is positioned longitudinally around the inner liner and bonded to the outer surface of the liner. The reinforcing member, which may be a triaxial braid, or an encapsulated longitudinal reinforcing wire, extends along the outer jacket length and is configured for inhibiting elongation of the sheath upon deployment of the device.

Abstract: A packaging tray for a medical device having a substantially flat configuration with at least one surface thereof comprising a coating of an agent disposed thereupon and an uncoated portion extending laterally therefrom. The packaging tray comprises a container unit having top and bottom portions that define a protective chamber therebetween configured to receive the coated portion of the medical device. The container unit is further configured to include an anchoring region disposed lateral to the protective chamber and between the top and bottom portions. When the medical device is disposed within the container unit, the uncoated portion is at least partially received and secured within the anchoring region, and the coated portion is maintained within the protective chamber, such that the coating of the agent is prevented from contacting the top and bottom portions of the container unit.

Abstract: A transparent packaging laminate (10) for use in a container (15) for protecting medical products (18) from oxidation and deterioration as a result of exposure to ultraviolet light. The laminate includes a first transparent film (11) of a polyethylene material laminated with a polyester adhesive (13) to a second transparent film (12) of a polyester material. The transparent polyethylene material has a water vapor transmission rate of less than 20 grams/m.sup.2 /24 hours. The transparent polyester material absorbs ultraviolet light having a wavelength in a range of from 285 to 358 nanometers and has a water vapor transmission rate greater than 20 grams/m.sup.2 /24 hours, whereby the resulting laminate is unexpectedly wrinkle-free after ethylene oxide sterilization.