Liaison™ XL Murex HIV Ab/Ag HT Assay - FDA Registration IVDR-00771

Access comprehensive regulatory information for Liaison™ XL Murex HIV Ab/Ag HT Assay in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00771 and manufactured by DiaSorin Italia S.p.A. Via Crescentino, snc 13040 Saluggia (VC) Italy in Italy. The device was registered on January 09, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifeline Diagnostics Supplies, 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.