ARCHITECT ANTI-HBs SPECIMEN DILUENT - FDA Registration IVDR-00477C

Access comprehensive regulatory information for ARCHITECT ANTI-HBs SPECIMEN DILUENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00477C and manufactured by Abbott Ireland Diagnostics Division - Finisklin Business Park, Sligo, Ireland in Ireland. The device was registered on March 08, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Abbott Laboratories), 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.