Castroviejo Caliper 9/20 - EUDAMED Registration G520MD16670

Access comprehensive regulatory information for Castroviejo Caliper 9/20 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 G520MD16670 and manufactured by Medspo in Pakistan.

This page provides complete registration details including trade name (Castroviejo Caliper 9/20), manufacturer information, authorized representative details, competent authority (DE/CA38 - Regierungspräsidium Karlsruhe), 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.