Reagents used for BenchMark GX System (10 Items) - FDA Registration 6b6020d8ea5bc670471cf4266129ba73
Access comprehensive regulatory information for Reagents used for BenchMark GX System (10 Items) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6b6020d8ea5bc670471cf4266129ba73 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
6b6020d8ea5bc670471cf4266129ba73
Reagents used for BenchMark GX System (10 Items)
FDA ID: 6b6020d8ea5bc670471cf4266129ba73
Device Classification
Brand Name
Window
Registration Information
Analysis ID
6b6020d8ea5bc670471cf4266129ba73
Registration Date
December 09, 2022
Manufacturer
Authorized Representative

