SYPHILIS CARD [Ultra Sensitive (IgG/IgM/IgA)] - FDA Registration 5933ad1256a83197f8ce24bbf8e651f0
Access comprehensive regulatory information for SYPHILIS CARD [Ultra Sensitive (IgG/IgM/IgA)] in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5933ad1256a83197f8ce24bbf8e651f0 and manufactured by Reckon Diagnostics Pvt, Ltd.. The device was registered on February 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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5933ad1256a83197f8ce24bbf8e651f0
SYPHILIS CARD [Ultra Sensitive (IgG/IgM/IgA)]
FDA ID: 5933ad1256a83197f8ce24bbf8e651f0
Device Classification
Brand Name
Reckon
Registration Information
Analysis ID
5933ad1256a83197f8ce24bbf8e651f0
Registration Date
February 15, 2022
Manufacturer
Authorized Representative

