MAGLUMI HBsAg (CLIA) Reagent Kit - FDA Registration d6cbe138ac65d73c40be659f0d4bbb7a
Access comprehensive regulatory information for MAGLUMI HBsAg (CLIA) Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d6cbe138ac65d73c40be659f0d4bbb7a and manufactured by Shenzhen New Industries Biomedical Engineering Co., Ltd.. The device was registered on August 20, 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
d6cbe138ac65d73c40be659f0d4bbb7a
MAGLUMI HBsAg (CLIA) Reagent Kit
FDA ID: d6cbe138ac65d73c40be659f0d4bbb7a
Device Classification
Brand Name
Snibe Diagnostic Brand
Registration Information
Analysis ID
d6cbe138ac65d73c40be659f0d4bbb7a
Registration Date
August 20, 2022
Manufacturer
Authorized Representative

