Radifocus GUIDE WIRE M - FDA Registration e55ef6030fd357f64f593c8d81d5b1ca

Access comprehensive regulatory information for Radifocus GUIDE WIRE M in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e55ef6030fd357f64f593c8d81d5b1ca and manufactured by Terumo Vietnam Co., Ltd.. The device was registered on December 19, 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.