Leptospira IgG/IgM Combo Rapid Test - FDA Registration 04fa668e0dd9761db66d555ffa203f71
Access comprehensive regulatory information for Leptospira IgG/IgM Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 04fa668e0dd9761db66d555ffa203f71 and manufactured by CTK Biotech, Inc.. The device was registered on September 01, 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
04fa668e0dd9761db66d555ffa203f71
Leptospira IgG/IgM Combo Rapid Test
FDA ID: 04fa668e0dd9761db66d555ffa203f71
Device Classification
Brand Name
Onsite
Registration Information
Analysis ID
04fa668e0dd9761db66d555ffa203f71
Registration Date
September 01, 2022
Manufacturer
Authorized Representative

