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"Ji Bo" low-frequency therapy device - Taiwan Registration 4bdc08510ade4dc2cc53e5d79c5e4913

Access comprehensive regulatory information for "Ji Bo" low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4bdc08510ade4dc2cc53e5d79c5e4913 and manufactured by Chemchem Technology Co., Ltd. Freshwater Plant;; HOBO CO., LTD. The authorized representative in Taiwan is Wellell Inc..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jimao Technology Co., Ltd. freshwater plant, and 1 recent registrations in the same category. 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.

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4bdc08510ade4dc2cc53e5d79c5e4913
Registration Details
Taiwan FDA Registration: 4bdc08510ade4dc2cc53e5d79c5e4913
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Device Details

"Ji Bo" low-frequency therapy device
TW: โ€œ้›ƒๅšโ€ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

4bdc08510ade4dc2cc53e5d79c5e4913

Company Information

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;; Contract manufacturing

Dates and Status

May 31, 2020

Apr 04, 2026

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