Huachenyang (Shenzhen) Technology Co., Ltd CY-B-F005-20 iClean

Table in great working condition. Moves up and down. Very tiny tear in vinyl (picture shown)

REUSABLE and STERILIZABLE device designed to remove a broken prosthetic screw from the inside of a dental implant.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.

Xpert Swab Specimen Collection Kit; 50 pack

Key features of the Baxter Hillrom Yellofin stirrups typically include: Lithotomy Positioning: Provides reliable lithotomy positioning with a boot-like design for the lower legs, allowing secure support while minimizing nerve stress. Self-adjusting Boot: The boot is designed to automatically adjust to the patient's anatomy, reducing the risk of pressure injuries. Lift Assist Mechanism: It features an assist mechanism to make leg adjustments smoother and easier for medical personnel. Enhanced Safety: Some models include a secure locking system that prevents unintentional adjustments during surgery. Durability: Made from high-grade materials to ensure longevity and withstand repeated sterilization. This system is widely used in OR environments for its precision and ergonomic advantages for both patients and clinicians.

Burr, Oval, 10 flute, 3.0mm

Dura-Cuf Inflation System - 2-Tube Blood Pressure Inflation System with Luer Slip, Infant

Table in great working condition. Moves up and down. Very tiny tear in vinyl (picture shown)

REUSABLE and STERILIZABLE device designed to remove a broken prosthetic screw from the inside of a dental implant.

The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.