Myanmar FDA registration 720c0f763f77387400c0b6247f79d1a4
Reagents used for e801 system (3 Items)
Myanmar·Roche·Roche Diagnostics (Suzhou) Ltd.·Registered December 16, 2022Device classification
- Brand Name
- Roche
Registration information
- Analysis ID
- 720c0f763f77387400c0b6247f79d1a4
- Registration Date
- December 16, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Reagents used for e801 system (3 Items) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 720c0f763f77387400c0b6247f79d1a4 and manufactured by Roche Diagnostics (Suzhou) Ltd.. The device was registered on December 16, 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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