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Activ Surgical Announces FDA Clearance for ActivSight Intraoperative Imaging Module

Activ Surgical announced the U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s ActivSight Intraoperative Imaging Module for enhanced surgical visualization.

Metrex Surface Disinfectant Portfolio Secures EPA Approval

The U.S. Environmental Protection Agency (EPA) has approved all eight surface disinfectant products made by an infection prevention leader, Metrex, as effective against SARS-CoV-2, the novel coronavirus that causes COVID-19.

Olympus Supports Safety Actions Regarding Surgical Smoke

Olympus has announced its support of The Joint Commission’s recommended safety actions for managing the hazards of exposure to surgical smoke for health care staff in operating rooms.

Exofin Fusion Redesign Receives FDA Approval

Chemence Medical, a leader in medical cyanoacrylate devices and products, announced the U.S. Federal Drug Administration’s (FDA) 510(k) approval of the company’s redesigned exofin fusion skin closure system.

Skytron Ergon Anesthesia Tether Skyboom

Skytron’s Ergon Anesthesia Tether Skyboom allows the utility supply boom to be tethered to the back of the anesthesia machine, making OR turnaround and room setup more efficient. having the boom tethered to the anesthesia machine decreases the overall footprint and makes relocating the anesthesia machine seamless. using the Ergon Anesthesia Tether Skyboom also helps increase workflow efficiency in the operating room. The design Skytron has incorporated in the Anesthesia Tether Skyboom allows the boom to be untethered from the machine in under a minute. This design is also favored by biomed personnel having minimal replaceable parts, the company says.

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