Angiographic Catheter (RADIFOCUS GLIDECATH) - FDA Registration 8183f1ef81b67e8615bda7f320497b91

Access comprehensive regulatory information for Angiographic Catheter (RADIFOCUS GLIDECATH) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8183f1ef81b67e8615bda7f320497b91 and manufactured by Ashitaka Factory of Terumo Corporation. The device was registered on November 10, 2021.

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.