STANDARD Q Yellow fever IgM - FDA Registration 31594ae1e57a3ce8ac936c00dd998285
Access comprehensive regulatory information for STANDARD Q Yellow fever IgM in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 31594ae1e57a3ce8ac936c00dd998285 and manufactured by SD Biosensor, Inc.. The device was registered on October 15, 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
31594ae1e57a3ce8ac936c00dd998285
STANDARD Q Yellow fever IgM
FDA ID: 31594ae1e57a3ce8ac936c00dd998285
Device Classification
Brand Name
STANDARD Q
Registration Information
Analysis ID
31594ae1e57a3ce8ac936c00dd998285
Registration Date
October 15, 2022
Manufacturer
Authorized Representative

