Centinel Spine®, LLC ("the Company"), the leading global medical device company focused exclusively on treating cervical and ...

The European Union’s Medical Device Regulation (MDR) is a complex regulatory framework created to put in place rules and requirements in how medical devices are designed, manufactured, and marketed.

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

Centinel Spine’s Prodisc C Vivo and Prodisc C Nova earned the European Union’s Medical Device Regulation certifications, according to a Sept. 11 news release. Prodisc C Vivo and C Nova are the only ...

DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...

Starting from today, the new Medical Device Regulation (MDR) replaces the Medical Device Directive (93/42/EEC) and Directive on Active Implantable Medical Devices (90/385/EEC) in the European Union.

LUND, Sweden, March 11, 2024 /PRNewswire/ -- Enzymatica's mouth spray ColdZyme® has received CE-certification under the new and more demanding European Union medical device regulation (MDR). This ...

Dublin, Feb. 17, 2025 (GLOBE NEWSWIRE) -- The "An Introduction to the Medical Device Regulation Training Course" conference has been added to ResearchAndMarkets.com's offering. This is an excellent ...

Compliance with the Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare ...