COBAS® TAQMAN® HIV-1 TEST V2.) KIT - FDA Registration IVDR-00325

Access comprehensive regulatory information for COBAS® TAQMAN® HIV-1 TEST V2.) KIT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00325 and manufactured by Roche Molecular Systems, Inc. in USA. The device was registered on June 14, 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.