"TERUMO" REDIFOCUS GLIDECATH - Taiwan Registration 98aa5c532e0e7eec127f3b6bd62a1697

Access comprehensive regulatory information for "TERUMO" REDIFOCUS GLIDECATH in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98aa5c532e0e7eec127f3b6bd62a1697 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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