Taiwan FDA registration 8cf775763fd6218cfda8d3b601de77ed
LOHAS Low Frequency Therapy Device
TW: 樂活貼低週波治療器
Taiwan·Risk Class 2·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Dec 22, 2022 – Dec 22, 2027ActiveRegistration details
- Analysis ID
- 8cf775763fd6218cfda8d3b601de77ed
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NU-BECA & MAXCELLENT CO.
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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Dec 22, 2022
- Expiry Date
- Dec 22, 2027
About this record
Access comprehensive regulatory information for LOHAS 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 8cf775763fd6218cfda8d3b601de77ed and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is NU-BECA & MAXCELLENT CO..
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