Visalis 500 and accessories - FDA Registration 0c6f3101fbb418b424582e5e1b9326c6

Access comprehensive regulatory information for Visalis 500 and accessories in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0c6f3101fbb418b424582e5e1b9326c6 and manufactured by Carl Zeiss Meditec AG. The device was registered on March 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.