STANDARD Q Zika IgM - FDA Registration b975dce2d048f42171c0702ff61cef74
Access comprehensive regulatory information for STANDARD Q Zika IgM in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b975dce2d048f42171c0702ff61cef74 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
b975dce2d048f42171c0702ff61cef74
STANDARD Q Zika IgM
FDA ID: b975dce2d048f42171c0702ff61cef74
Device Classification
Brand Name
STANDARD Q
Registration Information
Analysis ID
b975dce2d048f42171c0702ff61cef74
Registration Date
October 15, 2022
Manufacturer
Authorized Representative

