Pure Global

LOHAS Low Frequency Therapy Device - Taiwan Registration 8cf775763fd6218cfda8d3b601de77ed

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..

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
8cf775763fd6218cfda8d3b601de77ed
Registration Details
Taiwan FDA Registration: 8cf775763fd6218cfda8d3b601de77ed
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

LOHAS Low Frequency Therapy Device
TW: ๆจ‚ๆดป่ฒผไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

8cf775763fd6218cfda8d3b601de77ed

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

Domestic;; Contract manufacturing

Dates and Status

Dec 22, 2022

Dec 22, 2027