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STANDARD Q Rota/Adeno Ag - FDA Registration 2b6f81329a370f5eb8b38564d4fa909c

Access comprehensive regulatory information for STANDARD Q Rota/Adeno Ag in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2b6f81329a370f5eb8b38564d4fa909c and manufactured by SD Biosensor, Inc.. The device was registered on September 17, 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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2b6f81329a370f5eb8b38564d4fa909c
STANDARD Q Rota/Adeno Ag
FDA ID: 2b6f81329a370f5eb8b38564d4fa909c
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Device Classification
Brand Name
STANDARD Q
Registration Information
Analysis ID
2b6f81329a370f5eb8b38564d4fa909c
Registration Date
September 17, 2022
Manufacturer
Authorized Representative