Fistula Needles - FDA Registration 492e436ef04ebe52ec30f00a90752148

Access comprehensive regulatory information for Fistula Needles in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 492e436ef04ebe52ec30f00a90752148 and manufactured by Nipro (Thailand) Corporation Ltd.. The device was registered on July 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.