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"Ji Bo" low-frequency therapy device - Taiwan Registration ba6045340813a7d2803d719e2ead18bc

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 ba6045340813a7d2803d719e2ead18bc and manufactured by Jimao Technology Co., Ltd. freshwater plant. The authorized representative in Taiwan is Wellell Inc..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Chemchem Technology Co., Ltd. Freshwater Plant;; HOBO CO., LTD, 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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ba6045340813a7d2803d719e2ead18bc
Registration Details
Taiwan FDA Registration: ba6045340813a7d2803d719e2ead18bc
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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

ba6045340813a7d2803d719e2ead18bc

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Contract manufacturing;; Domestic

Dates and Status

May 07, 2021

May 06, 2024

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