Gingras Ligature Director - EUDAMED Registration G520MD45030

Access comprehensive regulatory information for Gingras Ligature Director 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 G520MD45030 and manufactured by Medspo in Pakistan.

This page provides complete registration details including trade name (Gingras Ligature Director), 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.