SARA FLEX - EUDAMED Registration 05059441438076

Access comprehensive regulatory information for SARA FLEX 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 05059441438076 and manufactured by ArjoHuntleigh AB in Sweden.

This page provides complete registration details including trade name (Maxi Move 5), manufacturer information, competent authority (Swedish Medical Products Agency), 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.