Sterile Single Use Peripheral Arteries Percutaneous Transluminal Angioplasty(PTA) Dilatation Catheter - EUDAMED Registration 06935456205829

Access comprehensive regulatory information for Sterile Single Use Peripheral Arteries Percutaneous Transluminal Angioplasty(PTA) Dilatation Catheter 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 06935456205829 and manufactured by Princeton Medical Scientific Co.,Ltd in China.

This page provides complete registration details including trade name (Principal® Peripheral Arteries Percutaneous Transluminal Angioplasty(PTA) Dilatation Catheter ), manufacturer information, authorized representative details, competent authority (The Medicines and Healthcare Products Regulatory 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.