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Reagents used in BenchMark GX System (2 Items) - FDA Registration 49295aadc060ff4aae62df22e33c318b

Access comprehensive regulatory information for Reagents used in BenchMark GX System (2 Items) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 49295aadc060ff4aae62df22e33c318b and manufactured by Ventana Medical Systems, Inc.. The device was registered on August 02, 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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49295aadc060ff4aae62df22e33c318b
Reagents used in BenchMark GX System (2 Items)
FDA ID: 49295aadc060ff4aae62df22e33c318b
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Device Classification
Brand Name
Ventana Brand
Registration Information
Analysis ID
49295aadc060ff4aae62df22e33c318b
Registration Date
August 02, 2022
Authorized Representative