COBAS® TAQMAN GHB TEST - FDA Registration IVDR-00331A

Access comprehensive regulatory information for COBAS® TAQMAN GHB TEST in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00331A and manufactured by Roche Molecular Systems, Inc. in USA. The device was registered on May 16, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Roche (Philippines), Inc.), 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.