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.

Spacelabs DM4

Spacelabs Healthcare’s DM4 dual-mode monitor is the newest member of the company’s patient monitoring line. The DM4 is designed for use in any patient care environment where basic vital signs monitoring is needed, and it is expected to enable caregivers to adapt to changes in patient condition without having to locate additional equipment. In spot-check mode, the DM4 can wirelessly transmit individual patient records to an electronic medical record system (EMR), or it can be used to efficiently collect and download multiple patients’ records in batch mode from a central location. If more vigilance is required, the DM4 can be quickly switched to continuous monitoring mode with alarm notification support.



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