Single Use Guidewire - FDA Registration f9f1cb1c985e9c20ecdb6799d9bf317d

Access comprehensive regulatory information for Single Use Guidewire in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f9f1cb1c985e9c20ecdb6799d9bf317d and manufactured by Ashitaka Factory of Terumo Corporation. The device was registered on November 19, 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.