Resyca Receives Medical Device Regulation Certificate From TÜV SÜD
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
Business Wire22 天
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical ...
The introduction of the Person Responsible for Regulatory Compliance (PRRC) role mandated under the Medical Device Regulation (MDR) 2017/745 and the ... documentation for EU and global submissions ...
来自MSN11 个月
X-Nav Technologies' X-Guide® System First to Receive EU Medical Device Regulation ...
has announced that its X-Guide® Dynamic 3D Surgical Navigation System is the first of its kind to receive certification under the European Union Medical Device Regulation 2017/745, also known as ...
Radformation’s Automation Solutions Achieve MDR CE Mark
Radformation Inc., a global pioneer in radiation oncology software solutions, is proud to announce that AutoContour, ClearCheck, ClearCalc, and ChartCheck have achieved the EU Medical Device ...
Taiwan News1 个月
Corvia Medical Achieves CE Certification for Atrial Shunt Under New EU MDR Standards
announced today that it has achieved CE certification for the Corvia® Atrial Shunt System under the latest EU Medical Device Regulations (EU MDR 2017/745). The Corvia Atrial Shunt is a catheter-based ...
PharmiWeb12 天
Progress in the MDR process - aap receives MDR certificate
Regulatory Approval/MiscellaneousProgress in the MDR process - aap receives MDR certificate 27.01.2025 / 14:00 CET/CESTThe issuer is solely responsible for the content of this announcement.aap ...