CE Marking: MDR and IVDR – all classifications
Helping Medical Device Startups Break Into the UK, EU, USA & GCC Markets
No challenge is too big!Simplimedica has years of experience with CE marking devices under MDD, IVDD, and more recently, the MDR and IVDR classifications. Your device may be –
- Sterile/Non-Sterile
- Invasive/ Non Invasive
- Active/ Active Implantable
- Software
- Drug-Device combination
- Biologic
- Point of care/self test
- IVD
We have worked with all device combinations. Please check in with us today to confirm that your product is a Medical Device and what the next steps to conformity are.
Not sure which service is right for you?
25+ Years of Regulatory Experience
We’re here to help
info@simplimedica.com