cobas® HIV-1/HIV-2 Qualitative Control Kit - FDA Registration IVDR-00905

Access comprehensive regulatory information for cobas® HIV-1/HIV-2 Qualitative Control Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00905 and manufactured by Roche Molecular System, Inc. – 1080 US Highway 202 South, Branchburg, New Jersey 08876, USA in USA. The device was registered on October 30, 2024.

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.