Myanmar FDA registration d535c83154df250880694679ee3e20c0
Patient Monitor
Myanmar·bistos·Bistos Co.,Ltd.·Registered July 22, 2022Device classification
- Brand Name
- bistos
Registration information
- Analysis ID
- d535c83154df250880694679ee3e20c0
- Registration Date
- July 22, 2022
Manufacturer
- Name
- Bistos Co.,Ltd.
Authorized Representative
About this record
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 d535c83154df250880694679ee3e20c0 and manufactured by Bistos Co.,Ltd.. The device was registered on July 22, 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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