Patient Monitor
MyanmarBistosBistos Co.,LtdRegistered June 23, 2022
VerifiedFDA Myanmar · official registry
Device classification
- Brand Name
- Bistos
Registration information
- Analysis ID
- cd12b8a6531b51a80caf1cae3603fbb6
- Registration Date
- June 23, 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 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.