Sterile & Non-Sterile Single Use Surgical Forceps - EUDAMED Registration +G628SB3015116000

Access comprehensive regulatory information for Sterile & Non-Sterile Single Use Surgical Forceps in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI +G628SB3015116000 and manufactured by Sehar Batool International in Pakistan.

This page provides complete registration details including trade name (Sterile Single-use Rochester Pean Artery Forceps, Straight, 16cm), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.