MAGLUMI® Syphilis (CLIA) - FDA Registration b9db6112e876b157e5afcae7105166e2
Access comprehensive regulatory information for MAGLUMI® Syphilis (CLIA) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b9db6112e876b157e5afcae7105166e2 and manufactured by Shenzhen New Industries Biomedical Engineering Co., Ltd.. The device was registered on November 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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b9db6112e876b157e5afcae7105166e2
MAGLUMI® Syphilis (CLIA)
FDA ID: b9db6112e876b157e5afcae7105166e2
Device Classification
Brand Name
Maglumi
Registration Information
Analysis ID
b9db6112e876b157e5afcae7105166e2
Registration Date
November 15, 2022
Manufacturer
Authorized Representative

