Austin, United States, April 15, 2026 (GLOBE NEWSWIRE)-- As per the SNS Insider report the Medical Device Reprocessing Market size was estimated at USD 2.63 billion in 2025 and is expected to reach ...
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 ...
Regulated medical device reprocessing is an important tool in improving environmental and public health outcomes, according to a new analysis published in Health Affairs. Health care systems generate ...
The lifespan of medical devices is growing longer as more and more hospitals are turning to device reprocessing to cut costs, reduce waste and maximize potential use of these items. Millions of single ...
Allow me to set the stage. Our plaintiff claims he felt a nagging pain in his shoulder for months and finally went to see the local orthopedic surgeon. The surgeon apparently informed him that the ...
The Emergency Care Research Institute (ECRI Institute) has released its annual "Top 10 Patient Safety Concerns for Healthcare Organizations," naming some repeat offenders—like device reprocessing—to ...
The established environmentalism mantra of “reduce, re-use, recycle” opened the door for medical device manufacturers to roll out recycling programs under the guise of sustainability efforts. But, in ...
MUNDELEIN, Ill.--(BUSINESS WIRE)--Medline, a global medical supplies distributor and manufacturer, today announced a new agreement with Novation, a leading health care services company serving the ...
WASHINGTON & BERLIN--(BUSINESS WIRE)--When health systems and hospitals use regulated reprocessed “single-use” devices, they reduce procedure costs without compromising patient safety, build supply ...
Grist is a nonprofit, independent media organization dedicated to telling stories of climate solutions and a just future. In 2015, a marine biologist filmed her team removing a plastic straw from a ...
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 ...
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, ...
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