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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..

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c8617271ee11abc82b69908b0186bac4
Registration Details
Taiwan FDA Registration: c8617271ee11abc82b69908b0186bac4
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Device Details

Likang medium frequency pulse therapy instrument
TW: ๅˆฉๅบทไธญ้ ป่„ˆ่กๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

c8617271ee11abc82b69908b0186bac4

DHY00500264400

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

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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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