I will perform eudamed registration for eu mdr devices

EUDAMED MANDATORY DEADLINE: MAY 28, 2026

For US manufacturers, the voluntary period is over for EU MDR CE marked devices. As of May 2026, EUDAMED registration is a hard requirement. No SRN and no UDI registration means your products can be stopped at the EU border!

I provide the technical execution to secure your market access. I am a US-based Regulatory Specialist with 13 years of experience, helping clients navigate EU MDR CE marking since its inception. I perform the actual portal work.

What I Provide:

• Proof of Registration: Official proof of submission and registration status. Steps included in this process are:

1. Actor Registration: Technical setup to secure your SRN.
2. UDI Device Registration: Mandatory entry for your first device (MDR/IVDR).
3. EMDN Mapping: Assigning required nomenclature codes.
4. AR Coordination: Managing the verification "handshake" with your EU Rep.

Why Choose The Manfredi Consulting Group?

• MDR Veterans: We've been managing MDR transitions since day one.
• Technical Doers: We perform the work ourselves. No outsourcing!
• US Based: Expert support in your time zone, and english is our native language. We are readily available to clients.