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ATELLICA IM HEPATITIS B E ANTIGEN QUALITY CONTROL (HBeAg QC) - FDA Registration IVDR-00897B

Access comprehensive regulatory information for ATELLICA IM HEPATITIS B E ANTIGEN QUALITY CONTROL (HBeAg QC) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00897B and manufactured by Siemens Healthcare Diagnostics Inc. - 511 Benedict Avenue, Tarrytown, NY, 10591, United States in United States. The device was registered on October 30, 2024.

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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United States
IVDR-00897B
ATELLICA IM HEPATITIS B E ANTIGEN QUALITY CONTROL (HBeAg QC)
Registered medical device in Philippines
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Device Information
Product Name
ATELLICA IM HEPATITIS B E ANTIGEN QUALITY CONTROL (HBeAg QC)
Registration Number
IVDR-00897B
Importer & Distribution
Importer/Distributor
Siemens Healthcare Inc.
Registration Dates
Issuance Date
October 30, 2024
Expiry Date
October 30, 2025