CliniSys, Inc 6.3 Sunquest Mitogen Genetics

Multiple Used Smith and Nephew Arthroscopy Towers in good condition. CAN BE SOLD SEPARATELY These Smith and Nephew Arthroscopy Towers are a comprehensive system designed for arthroscopic surgeries, providing high-quality imaging and efficient management of surgical procedures. Key components of the system include: LCD Monitor (Model: LMD-X310MD, SN: 8000251): This monitor offers crisp and clear display capabilities, essential for viewing real-time surgical images and videos during procedures. Its high-resolution screen ensures optimal visualization for surgical precision. S&N LENS Integrated System (REF: 72204354, SN: EEI063): This integrated system includes advanced lenses optimized for arthroscopic procedures, enhancing clarity and detail in imaging. It contributes to improved visualization of the surgical site, aiding in accurate diagnosis and treatment. S&N 660HD-E Image Management System (REF: 72204668, SN: EEO1193): The image management system plays a vital role in storing, organizing, and retrieving surgical images and videos. It offers streamlined workflow management, allowing surgeons to efficiently access and review patient data during and after procedures. Sony AC Adaptor (Model: AC-300MD, SN: 6401H617): The AC adaptor provides reliable power supply to the various components of the arthroscopy tower, ensuring uninterrupted operation throughout surgical procedures. Its compatibility with the system components enhances overall reliability and performance. Sony Digital Color Printer (Model: UP-DR80MD, SN: 731682): This digital color printer is utilized for printing high-quality images captured during arthroscopic surgeries. It offers fast and efficient printing capabilities, enabling surgeons to create detailed documentation of procedures for reference and patient records.

"ROCHESTER OCHNER FORCEPS 6-1/4"" 1X2"

"ROCHESTER OCHNER FORCEPS 8"" STR 1X2"

Osseoflex® CD-H Hydraulic Cement Delivery system is a bone cement delivery device designed to allow the physician to keep a safer distance from the radiation source during the cement delivery phase in vertebroplasty, vertebral augmentation procedures and the skeletal system.

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.

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 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 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. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images.