CONVEEN LATEX URISHEATH (SELF-SEALING) - FDA Registration MDR-01139

Access comprehensive regulatory information for CONVEEN LATEX URISHEATH (SELF-SEALING) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01139 and manufactured by Coloplast (Hongkong) Ltd. in Denmark. The device was registered on April 10, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Completesolution Pharmacy & General Merchandise), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.