“CoreSculpt” Electromagnetic Therapy Stimulator - Taiwan Registration 9d5f5da41e9a8ecdbc5911bce8455497

Access comprehensive regulatory information for “CoreSculpt” Electromagnetic Therapy Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d5f5da41e9a8ecdbc5911bce8455497 and manufactured by K1MED Co., Ltd. The authorized representative in Taiwan is Taike Medical Technology Co.,Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.