ARCHITECT HAVAb IgM Reagent Kit - FDA Registration 56bd188f1744155cb8c6c55760505938
Access comprehensive regulatory information for ARCHITECT HAVAb IgM Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 56bd188f1744155cb8c6c55760505938 and manufactured by Abbott GmbH. The device was registered on December 08, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
56bd188f1744155cb8c6c55760505938
ARCHITECT HAVAb IgM Reagent Kit
FDA ID: 56bd188f1744155cb8c6c55760505938
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
56bd188f1744155cb8c6c55760505938
Registration Date
December 08, 2022
Manufacturer
Name
Abbott GmbHAuthorized Representative

