A test technician prepares for an EMC test in a 10-m semianechoic chamber. Use of a semianechoic chamber is necessary for the immunity testing required under EN 60601-1-2:2001 for applicable medical ...
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 ...
EMC is fundamentally about peaceful coexistence: An electrical device must function correctly in the presence of interfering signals and not unduly disturb the environment with its own emissions.
Expertise from Forbes Councils members, operated under license. Opinions expressed are those of the author. In 2023, the Food and Drug Administration (FDA) took a more active approach to medical ...
DUBLIN--(BUSINESS WIRE)--The "Medical Device Regulations in Asia-Pacific Markets Training Course (Nov 3rd - Nov 4th, 2025)" training has been added to ResearchAndMarkets.com's offering. With the ...
Due to the increasing concerns about medical devices' cybersecurity risks, European Union regulators put forward a new set of market entry requirements for medical devices and in vitro diagnostic ...
Medical software is the backbone of modern healthcare, supporting electronic health records (EHRs), diagnostic systems, imaging technologies and embedded software in medical devices like pacemakers ...
CHALFONT SAINT PETER, England--(BUSINESS WIRE)--A research report from RWS, the world’s leading provider of technology-enabled language, content management and intellectual property services, ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback