Since the European Union’s main aims include consumer protection and ensuring product safety, you might be forgiven for thinking that the EU’s rules in those areas would be clear and straightforward.
The CE Marking approval indicates that a medical device meets the requirements of the European Medical Devices Directive. Until now, Materialise’s personalized devices made use of the custom-made ...
PARIS--(BUSINESS WIRE)--Regulatory News: CARMAT (FR0010907956, ALCAR), designer and developer of the world’s most advanced total artificial heart, aiming to provide a therapeutic alternative for ...
HUNTINGTON BEACH, Calif., Dec. 15, 2010 (GLOBE NEWSWIRE) -- iTech Medical, Inc. (OTCBB:IMSU) (Frankfurt:0IM), a medical information technology company, announced today that it has received CE Mark ...
The European Union (EU) has adopted three new regulations that aim to modernize the “New Approach” or NRF (New Regulatory Framework) for EU directives. These regulations were adopted in 2008, and the ...
PITTSBURGH--(BUSINESS WIRE)--ClearCount Medical Solutions, a leader in patient safety solutions, announced today that it has received approval to affix the CE mark to its SmartSponge and SmartWand-DTX ...
MONTREAL, SoundBite Medical Solutions Inc. today announces it has received CE Marking for the SoundBite™ Crossing System, a unique and novel first-in-class wire-based technology that is intended for ...
Since the European Union’s main aims include consumer protection and ensuring product safety, you might be forgiven for thinking that the EU’s rules in those areas would be clear and straightforward.
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