Patent classifications
A61M2039/0063
Assemblies for identifying a power injectable access port
A power-injectable access port suitable for injecting contrast media therethrough at a rate of at least 1 milliliter per second. The access port includes a housing, a septum, a reservoir, and an outlet stem in fluid communication with the reservoir. The power-injectable access port is structured for accommodating a pressure developed within the reservoir of at least 35 psi. The septum may include a radiopaque material forming a selected pattern when an x-ray is taken through the septum. The pattern may identify the access port as capable of accommodating injection of contrast media at a rate of at least 1 milliliter per second and/or as capable of accommodating a pressure developed within the reservoir of at least 35 psi. The pattern may identify the location of the septum following implantation of the power-injectable access port.
Flow component for medical lines and related production method
An injection site for medical lines includes a tubular body made of molded plastic material within which an elastic element made of thermoplastic material is overmolded on an enlarged end of the tubular body. The enlarged end delimits an inner annular flange and is formed with at least one radial through-hole through which the elastic element is overmolded in order to rest axially against the inner annular flange and fill the radial through-hole with an appendage.
MEDICAL CONNECTORS AND METHODS OF USE
A medical connector for use in a fluid pathway includes a substantially transparent housing having a proximal end with a proximal opening and a distal end with a distal opening, and a cavity extending therebetween. The connector provides a substantially visible fluid flow path extending through a substantial portion of the connector.
Medical connectors and methods of use
A medical connector for use in a fluid pathway includes a substantially transparent housing having a proximal end with a proximal opening and a distal end with a distal opening, and a cavity extending therebetween. The connector provides a substantially visible fluid flow path extending through a substantial portion of the connector.
Systems and methods to compensate for compression forces in an intravascular device
A system and method for providing vent channel geometries to compensate for compression forces experienced by a septum within an intravascular device.
Low Profile Venous Access Port Assembly
A venous access port assembly (10) having a housing base (28) with a discharge stem (16), a septum (14) and a cap (36). An interior reservoir (22) is defined by a well (30) in the housing base and the bottom surface of the septum, and a passageway (20) extends from the reservoir through the discharge stem (16). The cap (36) is secured to the housing base (28) and securely retains the septum in the assembly (10), compressing an annular flange (44) of the septum against a septum seat (46) of the housing base. Horizontal ribs on the interior of the cap snap into complementary grooves on the side wall of the housing base to mechanically lock together the cap and housing base during curing of the solvent bonding agent. The cap (48) is mechanically secured to the housing base (28) as well as being bonded thereto. Crush ribs (72) on the interior surface (68) of the cap (36), precisely center the cap about the housing base during assembly and compensating for manufacturing tolerances.
CONNECTOR AND INFUSION SET
A connector includes an elastic valve body that includes a top face on which a slit is formed and a bottom face opposite the top face; and a holding section that is in contact with the top face and the bottom face of the elastic valve body and holds the elastic valve body. The holding section surrounds the slit, and the elastic valve body includes a peripheral section that is positioned outward of a portion of the elastic valve body that is held by the holding section when the elastic valve body is viewed from the top face side. The elastic valve body and the holding section are configured such that a volume of the peripheral section in a state in which the elastic valve body is held by the holding section is larger than a volume of the peripheral section in a state in which the elastic valve body is not held by the holding section.