Cobas 5800 - FDA Registration 9100f704db59ba6540459a9617eb8e21
Access comprehensive regulatory information for Cobas 5800 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9100f704db59ba6540459a9617eb8e21 and manufactured by Roche Diagnostics International Ltd. The device was registered on January 31, 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
9100f704db59ba6540459a9617eb8e21
Cobas 5800
FDA ID: 9100f704db59ba6540459a9617eb8e21
Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
9100f704db59ba6540459a9617eb8e21
Registration Date
January 31, 2022
Manufacturer
Authorized Representative

