Patient Monitor - FDA Registration cd12b8a6531b51a80caf1cae3603fbb6
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 cd12b8a6531b51a80caf1cae3603fbb6 and manufactured by Bistos Co.,Ltd. The device was registered on June 23, 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
cd12b8a6531b51a80caf1cae3603fbb6
Patient Monitor
FDA ID: cd12b8a6531b51a80caf1cae3603fbb6
Device Classification
Brand Name
Bistos
Registration Information
Analysis ID
cd12b8a6531b51a80caf1cae3603fbb6
Registration Date
June 23, 2022
Manufacturer
Name
Bistos Co.,LtdAuthorized Representative

