Diaclon ABO/Rh Newbonrs DVI+ - FDA Registration IVDR-00213

Access comprehensive regulatory information for Diaclon ABO/Rh Newbonrs DVI+ in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00213 and manufactured by Bio-Rad Laboratories (Singapore) Pte. Ltd. 3A International Business Park #11-10/16, ICON @IBP Tower B, Singapore Mfd By: Diamed GmbH - Cressier FR, Switzerland For: Diamed Holding GmbH - Cressier FR, Switzerland in Singapore. The device was registered on May 14, 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.