Abstract: A method of using a power-injectable port includes obtaining the power-injectable access port, attaching a catheter to an outlet stem of the power-injectable access port, and implanting the power-injectable access port and the catheter into a patient. The method further includes identifying the power-injectable access port following the implanting, inserting a distal end of a needle through the septum and into the reservoir, and injecting contrast media through the needle at a rate of at least one milliliter per second. The power-injectable 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 rated for injection of contrast media at a flow rate of at least 1 milliliter per second. The power-injectable access port is structured for operation at a pressure in the reservoir of at least 35 psi.

Abstract: A medical balloon includes a generally cylindrical barrel wall having proximal and distal ends disposed between tapered cone walls and neck walls with a fiber layer comprised of circumferentially wrapped ribbon-shaped fiber embedded in a continuous matrix of polymer material defining the tapered cone walls and barrel wall, wherein the distance between the fiber wraps defines a fiber pitch or density that varies over the working length of the barrel wall in non-linear increments, for example in step-wise increments over the length of the barrel wall.

Abstract: A non-compliant medical balloon may be changed from a deflated state to an inflated state by increasing the internal pressure within the balloon. The balloon comprises a balloon layer having an outer surface, the balloon layer including a base layer, a first reinforcing layer and a second reinforcing layer. The base layer is formed of a polymer material. The first reinforcing layer is one of either a plurality of discrete inelastic fibers oriented substantially parallel to the long axis of the balloon and a first layer of textile fabric material, the textile fabric material being one of a woven, knitted, braided and non-woven fabric. The second reinforcing layer is one of either at least one inelastic fiber wrapped around the circumference of the balloon substantially transverse to the long axis of the balloon and a second layer of textile fabric material, the textile fabric material being one of a woven, knitted, braided and non-woven fabric.

Abstract: A biopsy device includes a sample-receiving device with a cavity configured to receive at least one tissue sample. The sample-receiving device is movable between a first position and a second position. A liquid supply unit is configured to supply a flushing liquid. The liquid supply unit is operatively connected to the cavity of the sample-receiving device when the sample-receiving device is in the second position, and the liquid supply unit is disconnected from the cavity of the sample-receiving device when the sample-receiving device is not in the second position.

Abstract: A biopsy marking apparatus for placing a radiopaque marker at the location of a percutaneous biopsy. The biopsy marking apparatus comprises an introducer in combination with a radiopaque marker. The introducer ejects the radiopaque marker at the location of the biopsy. The introducer is configured to completely eject the radiopaque marker and prevent it from being subsequently drawn into the introducer as the introducer is removed from the biopsied tissue mass. The radiopaque marker has enhanced radiopaque characteristics and enhanced non-migration characteristics.

Abstract: A marking device according to one embodiment of the invention comprises a handle, a cannula having a cannula distal end and slidably mounted to the handle, and a stylet having a stylet distal end and slidably mounted to the handle in the cannula. The stylet distal end is spaced proximally of the cannula distal end to form a marker recess that receives an imaging marker. The marking device further comprises an actuator operably coupled to the cannula to effect retraction of the cannula into the handle following implantation of the imaging marker. The imaging marker can be implanted by advancing the stylet relative to the cannula to eject the imaging marker from the marker recess, or the cannula can be retracted relative to the stylet to expose the imaging marker.

Abstract: A marking device includes a handle defining a hollow interior, and a delivery assembly slidably mounted to the handle. The delivery assembly includes a cannula, a stylet assembly, an imaging marker, and an actuator. The cannula has a cannula distal end with a marker recess. The imaging marker is disposed within the marker recess. The actuator is operably coupled to the delivery assembly and is operable to transition the delivery assembly through at least three configurations: a first configuration characterized in that the cannula is positioned in an extended position and the stylet assembly is positioned in a ready position; a second configuration characterized in that the cannula is positioned in the extended position and the stylet assembly is positioned in an implant position; and a third configuration characterized in that the cannula is positioned in the retracted cannula position and the stylet is retracted into the handle.

Abstract: A biopsy device for obtaining tissue samples from human or animal tissue is optimized for the sampling of tissues that are resilient and difficult to cut using conventional approaches. The biopsy device includes a cutting cannula, an inner member including a toothed rack having a sharpened distal tip configured to be introduced into the body and a sample notch for receiving the at least one severed tissue sample, the inner member receivable in the cutting cannula, and a cutting mechanism configured for causing the cutting cannula to be longitudinally displaced in a distal direction from a first position at the proximal end of the sample notch exposing the sample notch, to a second position at the distal end of the sample notch, so as to sever said tissue sample from remaining body tissue at the harvesting site. The toothed rack may be a rotatable and may be rigid.

Abstract: An access port for subcutaneous implantation is disclosed. The access port may include a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. The access port may further include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. The subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on a molded insert that is sandwiched between base and cap portions of the access port so as to be visible after implantation via x-ray imaging technology.

Abstract: A drug coated inflatable balloon catheter (200) configured to vibrate is disclosed. The vibration can dislodge the drug from the balloon. The vibration can also improve delivery of the drug to deeper layers of a vessel wall. The balloon catheter can include one or more support wires. The support wires can be coupled to an ultrasound transmission member (120). The ultrasound transmission member can transmit ultrasonic vibrations to the support wires and/or the balloon wall.

Abstract: An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on an insert that is incorporated into the access port so as to be visible after implantation via x-ray imaging technology.

Abstract: A non-compliant fiber-reinforced medical balloon comprises a first fiber layer and a second fiber layer embedded in a continuous matrix of thermally-weldable polymer material defining a barrel wall, cone walls and neck walls. The fibers of the first fiber layer have a pattern of different lengths and are divisible into a first group and a second group based on length. The length of the fibers of the second group varies progressively in accordance to their proximity to the fibers of the first group; the fibers of the second group closest to the fibers of the first group being longer than the fibers of the second group further from the fibers of the first group. The fiber of the second fiber layer winds circumferentially around the longitudinal axis of the balloon substantially over the entire length of the balloon.

Abstract: A method of making an implantable medical device includes extruding a first ePTFE tube and a second ePTFE tube, cutting a plurality of slits in the first ePTFE tube, positioning a radially expandable support layer between the first and second ePTFE tubes so that the slits span portions of the support layer, and laminating the first ePTFE tube to the second ePTFE tube through openings in the support layer.

Abstract: A method of power injecting a contrast medium into a patient, including obtaining a power-injectable access port suitable for power injection. The power injectable access port includes a housing defining a reservoir, and a septum. The septum may include a self-sealing material, and a radiopaque material. The radiopaque material may form a selected pattern when an x-ray is taken through the septum for identifying the power-injectable access port as being suitable for power injection. The power-injectable access port may be structured for accommodating a pressure developed within the reservoir of at least 35 psi, and may be designed to accommodate a fluid flow rate of at least 1 milliliter per second. After implanting the power-injectable access port in the patient, the method may include imaging the power-injectable access port and confirming via the selected pattern in the septum that the power-injectable access port is suitable for injecting the contrast medium.

Abstract: An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on an insert that is incorporated into the access port so as to be visible after implantation via x-ray imaging technology.

Abstract: A tissue handling system includes a biopsy device configured to deliver at least one tissue sample to a location outside the body of a patient. A tissue storage container is separate from the biopsy device. A tissue collecting device is configured to releasably engage the biopsy device to receive the at least one tissue sample from the biopsy device. The tissue collecting device is configured to be disengaged from the biopsy device and engaged with the tissue storage container to deliver the at least one tissue sample to the tissue storage container.

Abstract: A method of operating a biopsy device includes providing a hollow needle having a longitudinal axis; moving a sample-receiving device received in the hollow needle from a retracted position to an extended position to expose a cavity in the sample-receiving device, the cavity configured to receive a tissue sample; displacing the hollow needle in a distal direction relative to the sample-receiving device to sever tissue received by the cavity of the sample-receiving device; moving a toothed flexible member along the longitudinal axis to move the sample-receiving device in the hollow needle from the extended position to the retracted position, the toothed flexible member having a proximal portion that extends proximal to the proximal end of the hollow needle; and receiving the proximal portion of the toothed flexible member in a helical coiling-up groove of a housing element when the sample-receiving device is moved to the retracted position.

Abstract: An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating.

Abstract: A non-compliant medical balloon may be changed from a deflated state to an inflated state by increasing pressure within the balloon. The non-compliant medical balloon is composed of randomly oriented fibers forming an angle. The angle remains substantially unchanged when the balloon changes from a deflated state to an inflated state.

Abstract: A catheter includes a balloon and a shaft having a coaxial portion including an outer tubular member having a bore, a transition neck, an access fitting adjacent the proximate end of the catheter shaft for directing a guidewire into the catheter shaft, an inflation port, a guidewire tubular member disposed coaxially in the outer tubular member, the outer tubular member and guidewire tubular member defining a first, annular inflation/deflation lumen fluid communication with the inflation port, at least one second inflation/deflation lumen separate from and non-coaxial with the guidewire tubular member and having a cross-sectional area less than the cross-sectional area of the first inflation/deflation lumen and opening at a proximate end into the first inflation/deflation lumen and at the distal end of the transition neck.