ALTERNA® UROSTOMY BAG - FDA Registration MDR-00642

Access comprehensive regulatory information for ALTERNA® UROSTOMY BAG in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00642 and manufactured by Coloplast (Hongkong) Ltd in Denmark. The device was registered on April 29, 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.