VITEK® 2 AST-N204 - FDA Registration 5aa41043974d73df4a503219d0a3ee68
Access comprehensive regulatory information for VITEK® 2 AST-N204 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5aa41043974d73df4a503219d0a3ee68 and manufactured by BIOMERIEUX, Inc.. The device was registered on November 01, 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
5aa41043974d73df4a503219d0a3ee68
VITEK® 2 AST-N204
FDA ID: 5aa41043974d73df4a503219d0a3ee68
Device Classification
Brand Name
Biomerieux
Registration Information
Analysis ID
5aa41043974d73df4a503219d0a3ee68
Registration Date
November 01, 2022
Manufacturer
Name
BIOMERIEUX, Inc.Authorized Representative

