VITEK® 2 NH - FDA Registration a01173ed8260875a3ae10daa03baace4
Access comprehensive regulatory information for VITEK® 2 NH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a01173ed8260875a3ae10daa03baace4 and manufactured by BIOMERIEUX, Inc.. The device was registered on October 19, 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
a01173ed8260875a3ae10daa03baace4
VITEK® 2 NH
FDA ID: a01173ed8260875a3ae10daa03baace4
Device Classification
Brand Name
Biomerieux
Registration Information
Analysis ID
a01173ed8260875a3ae10daa03baace4
Registration Date
October 19, 2022
Manufacturer
Name
BIOMERIEUX, Inc.Authorized Representative

