Vital Connect, Inc. 6200-03 VistaCenter

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.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 its 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.

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

GE OEC Elite CFD 31cm Flat Detector Super C-Arm - VAS 15 Software. GE OEC Elite CFD C-Arm 31 cm Flat Detector w/ Bumper VAS 15 Vascular Software, SUPER C Motorized C Refurbished, Calibrated, Ready for Use 31 cm CMOS Flat Detector (CFD) - CMOS - Complementary metal-oxide semiconductor detector - DQE(0): 72% - Active amplification inside pixel for ultra-fast electron mobility - Active Matrix: 1548x1524 pixels - Pixel Pitch: 190.0 um - Nominal resolution (at display): 31 cm: 2.7 lp/mm; 21 cm: 2.8 lp/mm; 15 cm: 2.9 lp/mm - Quad-mode magnification: Live Zoom fluidly from 1 to 4X with no change in dose; Fixed try-mode Mag settings: 31cm/21cm/15cm Workstation Display - 13.6 in Live and Reference Image displayed size - 1 to 1 detail imaging chain from CMOS detector to 4K display resolution - Squircle shaped image retains 100% of image when rotated and no cropped or changed view. - 4K, 32" Ultra high definition (UHD) Color Display - Monitor displays two split screens for equivalent view of two 20in displays - 3840x2160 display resolution - 600 cd/m2 maximum brightness - Touchscreen interface with anti-reflection, anti-fingerprint - Easily position monitor to surgical line of sight with display mount on an articulating arm with five movements What's Included: GE OEC Elite CFD C-Arm, Super C; (REF OEC Elite) Qty: 1 GE Beam Limiting Device; (REF 5455288-03) Qty: 1 GE Laser Aiming Device; (REF 5440087) Qty: 1 GE Image Receptor; (REF 5457729-02) Qty: 1 GE Remote User Interface; (REF 5719003-01) Qty: 1 GE Hand Control OEC ELITE; (REF 5819193); Qty; 1 GE Foot Switch; (REF 1482807); Qty: 1 GE Skin Spacer - Squircular; (REF 5436688-01) Qty: 2

Used Oricare M7610 Patient Monitoring System in good condition. It offers real-time vital sign monitoring, a user-friendly touchscreen interface, customizable alarms, and seamless data storage and connectivity.

"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.

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.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 its 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.

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

GE OEC Elite CFD 31cm Flat Detector Super C-Arm - VAS 15 Software. GE OEC Elite CFD C-Arm 31 cm Flat Detector w/ Bumper VAS 15 Vascular Software, SUPER C Motorized C Refurbished, Calibrated, Ready for Use 31 cm CMOS Flat Detector (CFD) - CMOS - Complementary metal-oxide semiconductor detector - DQE(0): 72% - Active amplification inside pixel for ultra-fast electron mobility - Active Matrix: 1548x1524 pixels - Pixel Pitch: 190.0 um - Nominal resolution (at display): 31 cm: 2.7 lp/mm; 21 cm: 2.8 lp/mm; 15 cm: 2.9 lp/mm - Quad-mode magnification: Live Zoom fluidly from 1 to 4X with no change in dose; Fixed try-mode Mag settings: 31cm/21cm/15cm Workstation Display - 13.6 in Live and Reference Image displayed size - 1 to 1 detail imaging chain from CMOS detector to 4K display resolution - Squircle shaped image retains 100% of image when rotated and no cropped or changed view. - 4K, 32" Ultra high definition (UHD) Color Display - Monitor displays two split screens for equivalent view of two 20in displays - 3840x2160 display resolution - 600 cd/m2 maximum brightness - Touchscreen interface with anti-reflection, anti-fingerprint - Easily position monitor to surgical line of sight with display mount on an articulating arm with five movements What's Included: GE OEC Elite CFD C-Arm, Super C; (REF OEC Elite) Qty: 1 GE Beam Limiting Device; (REF 5455288-03) Qty: 1 GE Laser Aiming Device; (REF 5440087) Qty: 1 GE Image Receptor; (REF 5457729-02) Qty: 1 GE Remote User Interface; (REF 5719003-01) Qty: 1 GE Hand Control OEC ELITE; (REF 5819193); Qty; 1 GE Foot Switch; (REF 1482807); Qty: 1 GE Skin Spacer - Squircular; (REF 5436688-01) Qty: 2