STANDARD Q Tsutsugamushi IgM/IgG - FDA Registration e762b4212a42551f23aa215b4052f630
Access comprehensive regulatory information for STANDARD Q Tsutsugamushi IgM/IgG in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e762b4212a42551f23aa215b4052f630 and manufactured by SD Biosensor, Inc. The device was registered on December 03, 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
e762b4212a42551f23aa215b4052f630
STANDARD Q Tsutsugamushi IgM/IgG
FDA ID: e762b4212a42551f23aa215b4052f630
Device Classification
Brand Name
STANDARD Q
Registration Information
Analysis ID
e762b4212a42551f23aa215b4052f630
Registration Date
December 03, 2022
Manufacturer
Authorized Representative

