Philippines FDA registration MDR-00501A

ATELLICA™ IM HIV 1/0/2 ENHANCED (EHIV) ASSAY

Philippines·Siemens Healthcare GmbH·USA·Issued June 10, 2020 – June 10, 2021

Device information

Product Name: ATELLICA™ IM HIV 1/0/2 ENHANCED (EHIV) ASSAY
Registration Number: MDR-00501A

Manufacturer details

Manufacturer: Siemens Healthcare GmbH
Country of Origin: USA

Importer & distribution

Importer/Distributor: Siemens Healthcare Inc.

Registration dates

Issuance Date: June 10, 2020
Expiry Date: June 10, 2021

About this record

Access comprehensive regulatory information for ATELLICA™ IM HIV 1/0/2 ENHANCED (EHIV) ASSAY in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00501A 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.