Myanmar FDA registration 93821c97069d78cbab56fc210bca0fee
Patient Monitor
Myanmar·BISTOS·Bistos Co., Ltd·Registered April 21, 2022Device classification
- Brand Name
- BISTOS
Registration information
- Analysis ID
- 93821c97069d78cbab56fc210bca0fee
- Registration Date
- April 21, 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 93821c97069d78cbab56fc210bca0fee and manufactured by Bistos Co., Ltd. The device was registered on April 21, 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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