Some impressions of our lively discussions at #MEDICA2024 - the Leading International Trade Fair in hashtag#Düsseldorf.
Contact CERES anytime:
📧info@clinical-evaluations.com
📞+49 (0)7621/167333-0
Regulation (EU) 2023/607 extended the MDR transition period for medical devices compliant with 90/385/ECC or 93/42/ECC until 📆31 Dec. 2027 for class III and IIb (implantable) devices and until 📆31 Dec. 2028 for other class IIb, IIa and I (sterile/measuring function) devices, under certain conditions:
- A formal application for conformity assessment is required until 📅26 May 2024.
- A contract between the medical device manufacturer and a notified body on conformity assessment is required unt...
