RADIFOCUS GUIDE WIRE M "TERUMO" - Taiwan Registration bab9028b6e116293149ddd460828f3ad

Access comprehensive regulatory information for RADIFOCUS GUIDE WIRE M "TERUMO" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bab9028b6e116293149ddd460828f3ad and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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