Abstract: The present disclosure is directed to an endoscopic surgical instrument and methods for performing a diverticulum treatment. The surgical instrument includes a handle assembly, an elongated member and a jaw assembly. The elongated member is operably coupled to the distal end of the handle assembly, while the jaw assembly is operably coupled to a distal end of the elongated member. The jaw assembly includes a knife slot that is defined therewithin and is adapted to receive a knife blade to thereby cut tissue that is disposed between the jaw assembly. The jaw assembly is configured to approximate an esophageal tract and a diverticulum.

Abstract: An end effector assembly adapted to couple to an electrosurgical instrument, the end effector assembly including a pair of opposing jaw members pivotably attached about a pivot member and moveable from a first spaced position to a second grasping position. Each jaw member includes a jaw housing and a seal plate formed on an inner surface of the jaw member including at least two seal plate segments extending along a substantial portion of the length of the jaw members. An insulating member is positioned between adjacent seal plate segments and configured to provide electrical isolation between adjacent seal plate segments. Each sealing plate segment is adapted to selectively connect to an electrosurgical energy source and form part of an electrosurgical energy delivery circuit.

Abstract: A surgical instrument includes an end effector and a housing mechanically coupled to the end effector. The end effector includes a first actuating device configured to perform a first surgical procedure and a second actuating device integrally associated with the first actuating device and configured to perform a second surgical procedure, the second surgical procedure being independently operable and different than the first surgical procedure. An outer portion of the first actuating device and an outer portion of the second actuating device form a portion of an outer housing of the end effector. The housing includes a first actuator, mechanically coupled to the first actuating device and configured to impart movement to the first actuating device and a second actuator, mechanically coupled to the second actuating device and configured to impart movement to the second actuating device.

Abstract: A surgical system has a jaw assembly including a plurality of fasteners, an anvil and a drive beam for pushing an actuation sled. A drive screw imparts motion to the drive beam. An elongated body is configured to connect with the jaw assembly. A drive link connects a flexible drive shaft to the drive screw, the drive link being disposed off-axis. The jaw assembly and elongated body are separable from each other.

Abstract: A surgical stapler includes an anvil assembly and a cartridge assembly. The anvil assembly defines staple forming depressions. One or both of the anvil assembly and the cartridge assembly are pivotable relative to the other between an open position and a clamped position. The cartridge assembly includes a first plurality of staples and a second plurality of staples. The first plurality of staples is initially positioned in alignment with the staple forming depressions of the anvil assembly for ejection from the cartridge assembly. The second plurality of staples is movably supported in the cartridge assembly from a first position misaligned with the staple forming depressions of the anvil assembly to a second position aligned with the staple forming depressions for subsequent ejection from the cartridge assembly.

Abstract: An access port for the introduction of a needle cannula tip into an IV tube set includes a rigid tubular housing and a resilient member disposed adjacent an inlet of the housing. The resilient member includes an axial perforation extending through the resilient member, and is normally closed by the resilient character of the resilient member. A depression is defined in a proximal face of the resilient member, and includes sidewalls extending between the proximal face and the axial perforation to guide the tip of the cannulated needle toward the perforation as the cannulated needle is introduced into the access port.

Abstract: A forceps includes an end effector assembly having first and second jaw members, each jaw member including a tissue sealing plate disposed thereon. One or both of the jaw members is movable relative to the other between a spaced-apart position and an approximated position for grasping tissue therebetween. One or both of the jaw members defines a first channel extending therethrough and an opening in the tissue sealing plate thereof that is aligned with the first channel. A stop member having a pre-determined configuration is removably engaged within the first channel. At least a portion of the stop member is configured to extend through the opening of the tissue sealing plate to define a minimum gap distance between the tissue sealing plates of the jaw members when the jaw members are disposed in the approximated position.

Abstract: An ultrasonic surgical instrument includes a transducer assembly having a distal engagement member and configured to supply ultrasonic energy. A waveguide defines a longitudinal axis and has a proximal engagement member configured to threadingly engage the distal engagement member. The waveguide is configured to transmit the ultrasonic energy therealong to a distal end thereof for treating tissue. A torque member is coupled to the transducer assembly and is disposed about the longitudinal axis. The torque member is selectively rotatable about the longitudinal axis and relative to the waveguide to threadingly engage the transducer assembly and the waveguide to one another. The torque member includes a plurality of fingers pivotably coupled thereto and movable between a closed position and an open position. In the open position, each finger extends substantially perpendicularly from the longitudinal axis to define a moment arm that facilitates the engagement of the transducer assembly and the waveguide.

Abstract: An electronic thermometer includes a probe adapted to be heated by a subject for use in measuring a temperature of the subject. At least one temperature sensor detects a temperature of the probe. A probe sensor detects a condition at the probe. The probe sensor has an idle condition when the probe is not inserted into the subject. A processor is operatively connected to the probe sensor and programmed to monitor a change in the condition of the probe sensor from the idle condition to determine whether the probe has been received in a probe cover and inserted into the subject.

Abstract: A forceps includes an end effector assembly having first and second jaw members movable between a spaced-apart position and an approximated position for grasping tissue therebetween. A knife assembly having a cutting blade disposed at a distal end thereof is also provided. The knife assembly is translatable relative to the end effector assembly between a retracted position and an extended position, wherein the cutting blade extends between the jaw members to cut tissue grasped therebetween. The knife assembly includes a proximal component and a first distal component that includes the cutting blade. The proximal and first distal components are removably coupled to one another to facilitate replacement of the first distal component while the end effector assembly remains in a substantially assembled condition, i.e., without requiring substantial disassembly of the end effector assembly.

Abstract: A surgical instrument includes a shaft formed via extrusion. The shaft has one or more lumens extending therethrough. The lumen(s) each define a cross-sectional configuration. An end effector assembly is coupled to a distal end of the shaft. One or more components are coupled to the end effector assembly. The component(s) extend proximally from the end effector into the lumen(s) of the shaft. One or more of the components is formed via stamping. The component(s) define a cross-sectional configuration substantially complementary to the cross-section configuration of the lumen into which they extend.

Abstract: Medical devices and systems for treating a vascular condition are described. One such device includes a sheath, an elongate delivery member, and a lock. The sheath has a wall that includes an inner surface and an outer surface. The inner surface defines a lumen along the sheath. An access opening is in a proximal portion of the wall and is in fluid communication with the lumen. The delivery member is at least partially disposed within the lumen. The delivery member passes through the access opening. The lock is slidably disposed on an outer periphery of the wall. The lock slidably moves from a first position to a second position along a longitudinal axis of the sheath. The lock positioned in the first position restricts movement of the delivery member.

Abstract: A noise-suppressing electrocardiograph (ECG) adapter having a first end, a second end, and a noise-suppression element is presented, together with an ECG noise-suppressing system and related methods. In an embodiment, the noise-suppressing ECG adapter includes a housing having at least one first connector disposed at a first end of the housing adapted to electrically couple with an ECG lead set, and at least one second connector adapted for coupling to an input of an ECG device. The adapter includes a noise suppression element. The noise suppression element includes a ferromagnetic element having an opening defined therein. In an embodiment the noise suppression element is internal to the adapter. In another embodiment, the noise suppression element is tethered externally to the adapter and configured to clamp around at least a portion of an ECG leadwire.

Abstract: A compression garment assembly for applying compression therapy to a body part of a person. The compression garment assembly includes a compression garment, a controller, and a strap for mounting the controller on the compression garment. The controller includes structure configured for cooperating with the strap for mounting the controller on the compression garment. In one embodiment, the structure includes a mounting surface and first and second retainers on opposite sides of the mounting surface. A segment of the strap is receivable in an opening on the controller for mounting the controller on the compression garment.

Abstract: A catheter is disclosed. The catheter includes an elongated tubular body defining a longitudinal axis and extending to a distal end thereof, the tubular body having at least one lumen and a cuff disposed around the tubular body configured to contact tissue, the cuff formed from a plasma-treated material having enhanced tissue ingrowth properties.

Abstract: A vascular access system includes a vascular access device and a portable recirculation device. The vascular access device defines at least one lumen and is configured and dimensioned to be positioned within a blood vessel of a patient. The recirculation device includes a housing defining a channel having an inlet port and an outlet port for passage of blood through the channel. The channel includes a pump for circulating blood through the vascular access device.

Abstract: A compression sleeve configured for a conforming fit to a portion of a wearer's body, such as a leg. The compression sleeve includes at least one inflatable bladder. The sleeve has a periphery including at least six edges and is configured to wrap around the wearer's leg so that the bladder encircles the limb for applying compression therapy to the limb. The shape of the sleeve conforms to the limb of the wearer and keeps the sleeve in place on the limb.

Abstract: A medical device detachment system receives an elongate delivery member, having a lumen, and an elongate core member. The system includes a housing, a user input mechanism for receiving a user input to effect detachment of a medical device, such as an embolic coil, from a distal end of the delivery member, and a grasping mechanism for grasping and moving a proximal end of the core member relative to a proximal end of the delivery member. The system also includes a first sensor detecting positioning of the proximal end of the core member within the housing, and a second sensor, detecting movement of the grasping mechanism. An indicator is connected to the first and second proximity sensors and provides feedback to a user.

Abstract: A catheter includes an elongated tubular body including a first wall and second wall defining first and second lumens, respectively. Each wall extends to a distal end and defines a distal opening. The first and second walls may each include one or more side openings disposed proximal of the distal end. The first and second lumens are separated by a septum. The septum includes a septum extension extending distally from the septum. The septum extension is adapted to articulate relative to the septum in response to fluid flow into and out of the distal openings of the first and second lumens. The septum extension is dimensioned to partially obstruct fluid flow into the catheter through one of the distal openings upon the articulation of the septum extension.

Abstract: A compression garment having a sealable bladder pocket adapted for applying compression therapy to a selected body part of a patient. The compression garment includes a selectively inflatable bladder and a wrap having a selectively sealable pocket. The pocket has a sealable main opening sized for passing the bladder therethrough for inserting the bladder in the pocket and removing the bladder from the pocket. A connector on the bladder may be connected to a fluid supply line via the main opening. In other embodiments, the connector may be connected in fluid communication with the fluid supply line via a secondary opening separated from the main opening. Fluid is delivered from the fluid source to an inflatable interior of the bladder to impart compression therapy to the body part.