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 ...
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 ...
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 ...
The Association for the Advancement of Medical Instrumentation and the FDA hosted the 2011 Medical Device Reprocessing Summit to discuss challenges of reprocessing reusable medical devices. 1. Define ...
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 global single-use medical device reprocessing market is projected to grow at an impressive rate of 15% over the next five years. This growth is fueled by a combination of cost-saving needs within ...
In 2000, when FDA led the U.S. to become the first country in the world to regulate the use of reprocessed single-use devices, the agency responded to concerns from manufacturers and physicians that ...
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 ...
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 ...
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 ...
A Tennessee-based company specializing in medical device manufacturing and reprocessing plans to invest $1.2 million to expand its Norfolk operations, adding 60 jobs, the governor announced Friday.
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