One major change introduced by the EU MDR compared to the former European directives is the inclusion of products without an ...

THERACLION (ISIN: FR0010120402; Mnemo: ALTHE), an innovative company developing Sonovein®, a robotic platform for ...

Opportunities in the medical device market lie in mastering regulatory requirements and clinical evidence gathering for CE marking and compliance. Understanding data collection needs, conducting ...

AVON, Mass., May 13, 2025 /PRNewswire/ -- Cervos Medical, a wholly owned subsidiary of Ranfac Corp, is proud to announce the CERVOS® KeyPRP System has received official certification under the ...

LONDON--(BUSINESS WIRE)--Signifier Medical Technologies Limited (“Signifier”), a global leader in medical technology for sleep-disordered breathing, announces that it has achieved the EU MDR ...

DUBLIN--(BUSINESS WIRE)--The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. This intensive four-day ...

Neo Medical SA received certification under the EU Medical Device Regulation for its entire portfolio of spine surgical technologies. The approval means that the company can continue selling its ...

The request includes a call to postpone re-certification requirements for devices already certified under the medical ...

The company has completed registration and certification for its total disc replacement products, which are now CE-marked.

Signifier Medical Technologies Limited (“Signifier”), a global leader in medical technology for sleep-disordered breathing, announces that it has achieved the EU MDR certification for eXciteOSA®, its ...