ORTHO BIOVUE SYSTEM REVERSE DILUENT CASSETTE - FDA Registration IVDR-00371

Access comprehensive regulatory information for ORTHO BIOVUE SYSTEM REVERSE DILUENT CASSETTE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00371 and manufactured by Ortho-Clinical Diagnostics in USA. The device was registered on January 30, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Ortho-Clinical Diagnostics 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.