ATELLICA™ IM HIV 1/0/2 ENHANCED CONTROL (EHIV QC) - FDA Registration MDR-00501B

Access comprehensive regulatory information for ATELLICA™ IM HIV 1/0/2 ENHANCED CONTROL (EHIV QC) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00501B and manufactured by Siemens Healthcare GmbH in USA. The device was registered on June 10, 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.