Skip to content
info@kobridgeconsulting.com10FL, Kyobo Securities Building,97, Uisadang-daero, Yeongdeungpo-gu, 07327, Seoul, Korea+82 (0) 2 6336 6763
FacebookTwitterGoogle+LinkedinRss
Kobridge
Medical Device Consulting – Regulatory Affairs & Quality Assurance
KobridgeKobridge

Get in touch with us!
+82 (0) 2 6336 6763

  • Home
  • About Us
  • Our Services
  • News
  • Resources
  • Pricing
  • Testimonials
  • Contact
SEARCH
  • Home
  • About Us
  • Our Services
  • News
  • Resources
  • Pricing
  • Testimonials
  • Contact

Daily Archives: August 3, 2020

You are here:
  1. Home
  2. 2020
  3. August
  4. 03

Medical Device Classification in the EU MDR

Medical Device Classification in the EU MDR

CE MarkingBy NicolasAugust 3, 2020Leave a comment

Medical Device Classification in the EU MDR One of the first concerns for manufacturers of medical devices attempting to sell their products on the European market is to decide what class is suitable for their products. The Medical Device classification in the EU MDR of the product can affect how and when the notified body…

© kobridge Consulting - 2021. All rights reserved.
Go to Top