Vitek® 2 Compact 30 Clinical - FDA Registration aa0c4379512e5b8589ec993cff337347

Access comprehensive regulatory information for Vitek® 2 Compact 30 Clinical in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID aa0c4379512e5b8589ec993cff337347 and manufactured by BIOMERIEUX, Inc.. The device was registered on October 31, 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.