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Glucose (GLU) Reagent Kit (GOD-PAP Method) - FDA Registration e70340ff68ac0e44d0ab99249d035b1f

Access comprehensive regulatory information for Glucose (GLU) Reagent Kit (GOD-PAP Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e70340ff68ac0e44d0ab99249d035b1f and manufactured by CLINDIAG SYSTEMS Co., LTD. The device was registered on March 23, 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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e70340ff68ac0e44d0ab99249d035b1f
Glucose (GLU) Reagent Kit (GOD-PAP Method)
FDA ID: e70340ff68ac0e44d0ab99249d035b1f
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Device Classification
Brand Name
CLINDIAG
Registration Information
Analysis ID
e70340ff68ac0e44d0ab99249d035b1f
Registration Date
March 23, 2022
Authorized Representative