Reagents used in e411, e601, e602 System - FDA Registration 9ba33c6b8ccde7b23eb4655bf5e82144
Access comprehensive regulatory information for Reagents used in e411, e601, e602 System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9ba33c6b8ccde7b23eb4655bf5e82144 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
9ba33c6b8ccde7b23eb4655bf5e82144
Reagents used in e411, e601, e602 System
FDA ID: 9ba33c6b8ccde7b23eb4655bf5e82144
Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
9ba33c6b8ccde7b23eb4655bf5e82144
Registration Date
August 02, 2022
Manufacturer
Authorized Representative

