Taiwan FDA registration ba6045340813a7d2803d719e2ead18bc

"Ji Bo" low-frequency therapy device

TW: “雃博”低週波治療器
Taiwan flagTaiwan·Risk Class 2·Jimao Technology Co., Ltd. freshwater plant·Registered May 07, 2021 – May 06, 2024Expired
Registration details
Analysis ID
ba6045340813a7d2803d719e2ead18bc
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Wellell Inc.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
May 07, 2021
Expiry Date
May 06, 2024
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About this record

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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