ATELLICA™ IM SYPHILIS (SYPH) ASSAY - FDA Registration IVDR-00395A

Access comprehensive regulatory information for ATELLICA™ IM SYPHILIS (SYPH) ASSAY in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00395A and manufactured by Siemens Healthcare GmbH in USA. The device was registered on April 22, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Siemens Healthcare 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.