COBAS® TAQMAN® HCV TEST, V2.0 FOR USE WITH THE HIGH PURE SYSTEM - FDA Registration IVDR-00498

Access comprehensive regulatory information for COBAS® TAQMAN® HCV TEST, V2.0 FOR USE WITH THE HIGH PURE SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00498 and manufactured by Roche Molecular Systems, Inc. in Switzerland. The device was registered on June 10, 2020.

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.