Philippines FDA registration IVDR-00070

ADVIA CENTAUR HEPATITIS Be ANTIGEN (HBeAg) QUALITY CONTROL MATERIAL

Philippines·Siemens Healthcare GmbH·USA·Issued June 24, 2020 – March 28, 2025

Device information

Product Name: ADVIA CENTAUR HEPATITIS Be ANTIGEN (HBeAg) QUALITY CONTROL MATERIAL
Registration Number: IVDR-00070

Manufacturer details

Manufacturer: Siemens Healthcare GmbH
Country of Origin: USA

Importer & distribution

Importer/Distributor: Siemens Healthcare Inc.

Registration dates

Issuance Date: June 24, 2020
Expiry Date: March 28, 2025

About this record

Access comprehensive regulatory information for ADVIA CENTAUR HEPATITIS Be ANTIGEN (HBeAg) QUALITY CONTROL MATERIAL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00070 and manufactured by Siemens Healthcare GmbH in USA. The device was registered on June 24, 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.