Reagents used for e801 system (3 Items) - FDA Registration 720c0f763f77387400c0b6247f79d1a4
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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FDA Official Data
720c0f763f77387400c0b6247f79d1a4
Reagents used for e801 system (3 Items)
FDA ID: 720c0f763f77387400c0b6247f79d1a4
Device Classification
Brand Name
Roche
Registration Information
Analysis ID
720c0f763f77387400c0b6247f79d1a4
Registration Date
December 16, 2022
Manufacturer
Authorized Representative

