Fascial Dilator - FDA Registration b471907dd6a784ffa0d6e35878f5319b

Access comprehensive regulatory information for Fascial Dilator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b471907dd6a784ffa0d6e35878f5319b and manufactured by Marflow AG. The device was registered on November 16, 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.