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 ...
MONTREAL - Jubilant DraxImage Inc., a wholly owned subsidiary of Jubilant Pharma Limited, is pleased to announce the receipt of the CE Mark certificate for its state-of-the-art RUBY Rubidium Elution ...
EMBA Medical Ltd., headquartered in Dublin, Ireland, recently announced that it has received CE certification for its Hourglass™ Peripheral Embolization Plug as a Class IIb medical device. CE ...
The CDSCO has announced that all medical devices procured in India must have a valid license from a central or state ...
LE MONT-SUR LAUSANNE, Switzerland--(BUSINESS WIRE)--Regen Lab, a global commercial-stage medical technology company specializing in the research, development, registration, manufacturing and ...
The MDR CE certification is a more stringent requirement for medical devices than the previous Medical Device Directive (MDD), ensuring higher performance, quality standards, safety and clinical ...
CE mark or FDA approval? Medical device professionals weigh in With the ever-increasing stringency, time, and expense associated with FDA approval for medical devices, debate is sharpening in the ...
First Over-the-Wire Embolic Device Cleared for EU Commercial Release The Hourglass ™ Peripheral Embolization Plug is a class IIb medical device and will be manufactured in the EMBA Medical ™ Limited ...
Obtaining the CE certification under Medical Device Regulation reinforces Regen Lab’s positioning as a leading innovator of medical devices in the field of autologous tissue engineering therapies This ...
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