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Architect HBsAg Next Confirmatory Reagent Kit - FDA Registration IVDR-00939

Access comprehensive regulatory information for Architect HBsAg Next Confirmatory Reagent Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00939 and manufactured by Abott Ireland diagnostics division in Ireland. The device was registered on April 04, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Abbott Laboratories), 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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Ireland
IVDR-00939
Architect HBsAg Next Confirmatory Reagent Kit
Registered medical device in Philippines
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Device Information
Product Name
Architect HBsAg Next Confirmatory Reagent Kit
Registration Number
IVDR-00939
Manufacturer Details
Country of Origin
Ireland
Importer & Distribution
Importer/Distributor
Abbott Laboratories
Registration Dates
Issuance Date
April 04, 2025
Expiry Date
April 04, 2026