Creatinine Test Kit - FDA Registration 917e1192f3665c8bccc6382df6dee612
Access comprehensive regulatory information for Creatinine Test Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 917e1192f3665c8bccc6382df6dee612 and manufactured by ROBONIK (INDIA) PVT. LTD.. The device was registered on June 25, 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
917e1192f3665c8bccc6382df6dee612
Creatinine Test Kit
FDA ID: 917e1192f3665c8bccc6382df6dee612
Device Classification
Brand Name
Prietest
Registration Information
Analysis ID
917e1192f3665c8bccc6382df6dee612
Registration Date
June 25, 2022
Manufacturer
Authorized Representative

