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VITEK® 2 Reagents - FDA Registration 4eb433fab1e476254de5ebad11b27bda

Access comprehensive regulatory information for VITEK® 2 Reagents in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4eb433fab1e476254de5ebad11b27bda and manufactured by BIOMERIEUX, Inc.. The device was registered on May 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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4eb433fab1e476254de5ebad11b27bda
VITEK® 2 Reagents
FDA ID: 4eb433fab1e476254de5ebad11b27bda
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Device Classification
Brand Name
Biomerieux
Registration Information
Analysis ID
4eb433fab1e476254de5ebad11b27bda
Registration Date
May 02, 2022
Manufacturer
Authorized Representative