Reagents used in cobas c 701 System - FDA Registration 6c5a3901ee9243d71b7ab73b812926b6
Access comprehensive regulatory information for Reagents used in cobas c 701 System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6c5a3901ee9243d71b7ab73b812926b6 and manufactured by Roche Diagnostics (Suzhou) Ltd.. The device was registered on August 02, 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
6c5a3901ee9243d71b7ab73b812926b6
Reagents used in cobas c 701 System
FDA ID: 6c5a3901ee9243d71b7ab73b812926b6
Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
6c5a3901ee9243d71b7ab73b812926b6
Registration Date
August 02, 2022
Manufacturer
Authorized Representative

