Ankle foot orthosis - EUDAMED Registration 05052893002628
Access comprehensive regulatory information for Ankle foot orthosis in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05052893002628 and manufactured by Trulife Ltd in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (Matrix L-Pace AFO - Left Medium), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.
ENERGY RETURN ANKLE-FOOT ORTHOSES

