Reagents used in BenchMark GX System (6 Items) - FDA Registration a658c85abaa082eed3ac6328cf48be5f
Access comprehensive regulatory information for Reagents used in BenchMark GX System (6 Items) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a658c85abaa082eed3ac6328cf48be5f and manufactured by Ventana Medical Systems, Inc.. The device was registered on December 09, 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
a658c85abaa082eed3ac6328cf48be5f
Reagents used in BenchMark GX System (6 Items)
FDA ID: a658c85abaa082eed3ac6328cf48be5f
Device Classification
Brand Name
Ventana Brand
Registration Information
Analysis ID
a658c85abaa082eed3ac6328cf48be5f
Registration Date
December 09, 2022
Manufacturer
Authorized Representative

