VITROS IMMUNODIAGNOSTIC PRODUCTS HBeAg REAGENT PACK - FDA Registration RR-1720

Access comprehensive regulatory information for VITROS IMMUNODIAGNOSTIC PRODUCTS HBeAg REAGENT PACK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number RR-1720 and manufactured by Ortho-Clinical Diagnostics in United Kingdom. The device was registered on February 12, 2018.

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.