IH-QC 2 Internal Quality Control - FDA Registration IVDR-00711 B

Access comprehensive regulatory information for IH-QC 2 Internal Quality Control in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00711 B and manufactured by Bio-Rad Laboratories (Singapore) Pte. Ltd.- 3A International Business Park #11-10/16, ICON@IBP Tower B, Singapore 609935 Mfd by: DiaMed Holding GmbH- Pra Rond 23, 1785 Cressier FR Switzerland in Switzerland. The device was registered on August 10, 2023.

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.