Philippines FDA registration IVDR-00063

ADVIA CENTAUR HIV Ag/Ab COMBO (CHIV) ASSAY READY PACK

Name: ADVIA CENTAUR HIV Ag/Ab COMBO (CHIV) ASSAY READY PACK — Philippines FDA registration IVDR-00063
Creator: Siemens Healthcare GmbH
Keywords: ADVIA CENTAUR HIV Ag/Ab COMBO (CHIV) ASSAY READY PACK, IVDR-00063, Siemens Healthcare GmbH, Siemens Healthcare Inc., USA, Philippines FDA registration

PhilippinesSiemens Healthcare GmbHUSAIssued January 02, 2020 – August 31, 2022

VerifiedFDA Philippines · official registry

Device information

Product Name: ADVIA CENTAUR HIV Ag/Ab COMBO (CHIV) ASSAY READY PACK
Registration Number: IVDR-00063

Manufacturer details

Manufacturer: Siemens Healthcare GmbH
Country of Origin: USA

Importer & distribution

Importer/Distributor: Siemens Healthcare Inc.

Registration dates

Issuance Date: January 02, 2020
Expiry Date: August 31, 2022

About this record

Access comprehensive regulatory information for ADVIA CENTAUR HIV Ag/Ab COMBO (CHIV) ASSAY READY PACK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00063 and manufactured by Siemens Healthcare GmbH in USA. The device was registered on January 02, 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.