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Antibody Diluent - FDA Registration f89b594838622f6ccbf49fe07b0245cc

Access comprehensive regulatory information for Antibody Diluent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f89b594838622f6ccbf49fe07b0245cc and manufactured by Ventana Medical Systems, Inc.. The device was registered on November 26, 2021.

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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f89b594838622f6ccbf49fe07b0245cc
Antibody Diluent
FDA ID: f89b594838622f6ccbf49fe07b0245cc
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Device Classification
Brand Name
Ventana Brand
Registration Information
Analysis ID
f89b594838622f6ccbf49fe07b0245cc
Registration Date
November 26, 2021
Authorized Representative