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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.

ArjoHuntleigh Maxi AirTM

The Maxi Air™ is an air assisted single patient multiple use system that seeks to promote a safe and effective solution for lateral transfers. Lateral transfers and repositioning are the most commonly cited patient handling tasks reported in healthcare, but change is in the air. Maxi Air cushions the patient on a bed of air – a floating effect created by air flowing through the perforated underside of the inflatable single patient use mattress. This effect minimizes friction and shearing forces when transferring and repositioning the patient, resulting in a gentle and safe transfer for both the patient and caregiver. More information about ArjoHuntleigh can be found at www.arjohuntleigh.com.

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