Auriga XL 4007 (Laser System) - FDA Registration 2219134327374ec1216bcc62f0eeed9d

Access comprehensive regulatory information for Auriga XL 4007 (Laser System) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2219134327374ec1216bcc62f0eeed9d and manufactured by Boston Scientific Corporation. The device was registered on April 29, 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.