Percuflex TM Ureteral Stent - FDA Registration 900ef72abb67068043e267afe0bfe8b9

Access comprehensive regulatory information for Percuflex TM Ureteral Stent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 900ef72abb67068043e267afe0bfe8b9 and manufactured by Boston Scientific Corporation. The device was registered on August 05, 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.