ATELLICA™ IM HEPATITIS C (aHCV) ASSAY - FDA Registration IVDR-00485A
Access comprehensive regulatory information for ATELLICA™ IM HEPATITIS C (aHCV) ASSAY in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00485A and manufactured by Siemens Healthcare GmbH in USA. The device was registered on May 04, 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.
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USA
IVDR-00485A
ATELLICA™ IM HEPATITIS C (aHCV) ASSAY
Registered medical device in Philippines
Device Information
Product Name
ATELLICA™ IM HEPATITIS C (aHCV) ASSAY
Registration Number
IVDR-00485A
Manufacturer Details
Manufacturer
Siemens Healthcare GmbHCountry of Origin
USA
Importer & Distribution
Importer/Distributor
Siemens Healthcare Inc.Registration Dates
Issuance Date
May 04, 2020
Expiry Date
May 04, 2021

