Vitek 2 XL® - FDA Registration 456f40ae4fd06480126eb4cfbeaea4f3

Access comprehensive regulatory information for Vitek 2 XL® in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 456f40ae4fd06480126eb4cfbeaea4f3 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.