LN.AGE has a talented and experienced team dedicated to medical device companies and able to support you in developing your product, obtaining the CE-mark and entering the European market.
- » Design & Rapid Prototyping
- » CE – Marking
- » Preparation of the Device Technical File according
to MDD 2007/47/EC and applicable Standards
- » Negotiation with Notified Bodies and Ministry of Health
- » Post-market surveillance and reporting
- » Device Registration in Ministry of Health Database