Carbogen® Rapid Plasma Reagin (RPR) Card Test/Carbon Antigen for Syphilis Testing - FDA Registration IVDR-00984

Access comprehensive regulatory information for Carbogen® Rapid Plasma Reagin (RPR) Card Test/Carbon Antigen for Syphilis Testing in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00984 and manufactured by Tulip Diagnostics (P) Ltd. - Gitanjali, Tulip Block, Dr. Antonio Do Rego, Bagh, Alto Santacruz, Bambolim Complex P.O., Goa -403 402, India in India. The device was registered on July 01, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Biosite Medical Instruments), 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.