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Patient Monitor - FDA Registration cd2146f7c26f72dccc46ed1e014f0c03

Access comprehensive regulatory information for Patient Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cd2146f7c26f72dccc46ed1e014f0c03 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co.,ltd. The device was registered on November 18, 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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cd2146f7c26f72dccc46ed1e014f0c03
Patient Monitor
FDA ID: cd2146f7c26f72dccc46ed1e014f0c03
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Device Classification
Brand Name
Mindray
Registration Information
Analysis ID
cd2146f7c26f72dccc46ed1e014f0c03
Registration Date
November 18, 2022