Liquizyme Creatinine (Reagent kit) - FDA Registration eae91ce3d84000f72bb0065d02ca5f4c
Access comprehensive regulatory information for Liquizyme Creatinine (Reagent kit) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID eae91ce3d84000f72bb0065d02ca5f4c and manufactured by BEACON DIAGNOSTICS PVT.LTD.. The device was registered on October 08, 2021.
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
eae91ce3d84000f72bb0065d02ca5f4c
Liquizyme Creatinine (Reagent kit)
FDA ID: eae91ce3d84000f72bb0065d02ca5f4c
Device Classification
Brand Name
BEACON Brand
Registration Information
Analysis ID
eae91ce3d84000f72bb0065d02ca5f4c
Registration Date
October 08, 2021
Manufacturer
Authorized Representative

