cobas b 123 System - FDA Registration 758140d8e57becf4a13e58905ee4e9b1
Access comprehensive regulatory information for cobas b 123 System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 758140d8e57becf4a13e58905ee4e9b1 and manufactured by Roche Diagnostics International Ltd. The device was registered on July 28, 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
758140d8e57becf4a13e58905ee4e9b1
cobas b 123 System
FDA ID: 758140d8e57becf4a13e58905ee4e9b1
Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
758140d8e57becf4a13e58905ee4e9b1
Registration Date
July 28, 2022
Manufacturer
Authorized Representative

