MONOLISA™ HCV Ag-Ab Ultra V2 Testing Kit - FDA Registration IVDR-00143

Access comprehensive regulatory information for MONOLISA™ HCV Ag-Ab Ultra V2 Testing Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00143 and manufactured by Bio-rad Laboratories (Singapore) Pte. Ltd.- 3A International Business Park #11-10/16, ICON@IBP Tower B, Singapore 609935 Mfd. By: BIO-RAD- Route de Cassel - 59114 STEENVOORDE FRANCE For: BIO-RAD - 3 boulevard Raymond Poincaré, 92430 MARNES LA COQUETTE, France in France. The device was registered on October 04, 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.