Jack Egnatinsky, MD, medical director of the AAAHC and a retired anesthesiologist, discusses what ASCs must do to meet AAAHC standards if they reprocess single-use devices and equipment. Dr. Jack ...

The European Commission this week issued regulations establishing common specifications for the reprocessing of single-use medical devices under the Medical Device Regulation (MDR). Under MDR, ...

The European Commission (EC) on Tuesday set forth the common specifications (CS) for the reprocessing of single-use medical devices under the EU’s medical device regulation (MDR). The EC is proposing ...

Innovative Health, a leader in single-use device reprocessing, today highlighted the publication of a new workbook from CHARME, the Collaborative for Healthcare Action to Reduce MedTech Emissions, ...

In 2000, the FDA began to view and regulate all companies reprocessing single-use medical devices in the same way it viewed and regulated original equipment manufacturers (OEMs). Before returning ...

This article is written by Jason Wandersee, CEO of MEDISISS, a Medline-owned reprocessing company. MEDISISS is the leader in reprocessing to surgery centers throughout the United States since 1997.By ...

Duodenoscope-associated infections remain a safety concern, and single-use duodenoscopes have been introduced to mitigate ...

Every healthcare facility faces the same challenge: to reduce costs without sacrificing the delivery of quality care. As a result of dwindling healthcare reimbursements, and increased awareness of ...

FORT LIBERTY, NC-- Womack Army Medical Center (WAMC) received the prestigious Stryker Sustainability Solutions Environmental Excellence Platinum Award for its outstanding efforts in reprocessing ...