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UREA (Mod Berhelot) Test Kit - FDA Registration 93a0fc50bafcd31bb2ad5570fc87d241

Access comprehensive regulatory information for UREA (Mod Berhelot) Test Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 93a0fc50bafcd31bb2ad5570fc87d241 and manufactured by ROBONIK (INDIA) PVT. LTD.. The device was registered on October 26, 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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93a0fc50bafcd31bb2ad5570fc87d241
UREA (Mod Berhelot) Test Kit
FDA ID: 93a0fc50bafcd31bb2ad5570fc87d241
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Device Classification
Brand Name
Prietest
Registration Information
Analysis ID
93a0fc50bafcd31bb2ad5570fc87d241
Registration Date
October 26, 2021
Authorized Representative