Medical device labeling is considered as important as classifying a product or creating an insulation diagram. In IEC 60601-1, labeling is deemed "a critical ...

A medical device is an umbrella term for any instrument, software, or other article used alone or in combination for a medical purpose in humans. An estimated 2 million different kinds of medical ...

The Elena and Miles Zaremski Law Medicine Forum presents: Medical Device Regulation: Going from Bad to Worse...or Better? with George Horvath Innovations in medical device technology hold the ...

DUBLIN--(BUSINESS WIRE)--The "A Comprehensive View of FDA Regulations for Medical Devices" conference has been added to ResearchAndMarkets.com's offering. Don't let a common misunderstanding get you ...

The FDA said it could not find reason to impose new regulations on the servicing of medical devices, whether performed by original equipment manufacturers (OEMs), hospital systems or third-party ...

LE MONT-SUR LAUSANNE, Switzerland--(BUSINESS WIRE)--Regen Lab, a global commercial-stage medical technology company specializing in the research, development, registration, manufacturing and ...