cobas® HIV-1/HIV-2 Qualitative nucleic acid test for use on the cobas® 5800/6800/8800 - FDA Registration IVDR-00906

Access comprehensive regulatory information for cobas® HIV-1/HIV-2 Qualitative nucleic acid test for use on the cobas® 5800/6800/8800 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00906 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.