LIAISON XL HCG PREGNANCY REAGENT - FDA Registration IVDR-00335

Access comprehensive regulatory information for LIAISON XL HCG PREGNANCY REAGENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00335 and manufactured by DiaSorin Italia S.p.A Via Crescentino, snc 13040 Saluggia (VC) Italy in Italy. The device was registered on April 11, 2024.

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.