Myanmar FDA registration 650b4bf8a5ccb979c6d353c5e2969e77
Automated External Defibrillator
Device classification
- Brand Name
- Mindray
Registration information
- Analysis ID
- 650b4bf8a5ccb979c6d353c5e2969e77
- Registration Date
- March 25, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Automated External Defibrillator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 650b4bf8a5ccb979c6d353c5e2969e77 and manufactured by Shenzhen Mindray Bio- Medical Electronics Co.Ltd. The device was registered on March 25, 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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