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Reagents used for URIT automated hematology analyzers (L21, D31) - FDA Registration c94aa9ff8f043ca58c622121752d7399

Access comprehensive regulatory information for Reagents used for URIT automated hematology analyzers (L21, D31) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c94aa9ff8f043ca58c622121752d7399 and manufactured by URIT Medical Electronic Co., Ltd.. The device was registered on October 27, 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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c94aa9ff8f043ca58c622121752d7399
Reagents used for URIT automated hematology analyzers (L21, D31)
FDA ID: c94aa9ff8f043ca58c622121752d7399
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Device Classification
Brand Name
URIT Brand
Registration Information
Analysis ID
c94aa9ff8f043ca58c622121752d7399
Registration Date
October 27, 2022
Authorized Representative