VITEK® 2 AST-N405 - FDA Registration d99a323d249747d9bb99ad8da8f602e5
Access comprehensive regulatory information for VITEK® 2 AST-N405 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d99a323d249747d9bb99ad8da8f602e5 and manufactured by BIOMERIEUX, Inc.. The device was registered on October 24, 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
d99a323d249747d9bb99ad8da8f602e5
VITEK® 2 AST-N405
FDA ID: d99a323d249747d9bb99ad8da8f602e5
Device Classification
Brand Name
Biomerieux
Registration Information
Analysis ID
d99a323d249747d9bb99ad8da8f602e5
Registration Date
October 24, 2022
Manufacturer
Name
BIOMERIEUX, Inc.Authorized Representative

