Likang medium frequency pulse therapy instrument - Taiwan Registration c8617271ee11abc82b69908b0186bac4
Access comprehensive regulatory information for Likang medium frequency pulse therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8617271ee11abc82b69908b0186bac4 and manufactured by T.Y. SHERRY INTERNATIONAL CO., LTD.. The authorized representative in Taiwan is T.Y. SHERRY INTERNATIONAL 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.
Device Details
Registration Details
c8617271ee11abc82b69908b0186bac4
DHY00500264400
Product Details
For details, it is Chinese approved copy of the imitation order
K Neuroscience
K.5890 Transcutaneous electrical nerve stimulator for pain relief
Domestic
Dates and Status
Feb 23, 2009
May 27, 2019
Jun 22, 2022
Cancellation Information
Logged out
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