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“UNIPAD” neckare TENS device - Taiwan Registration 7d960030ef211a0e7b1f5485677a0e4d

Access comprehensive regulatory information for “UNIPAD” neckare TENS device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d960030ef211a0e7b1f5485677a0e4d and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is HIVOX BIOTEK INC..

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.

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7d960030ef211a0e7b1f5485677a0e4d
Registration Details
Taiwan FDA Registration: 7d960030ef211a0e7b1f5485677a0e4d
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Device Details

“UNIPAD” neckare TENS device
TW: “優尼帕德”頸掛型低周波治療器
Risk Class 2
MD

Registration Details

7d960030ef211a0e7b1f5485677a0e4d

Ministry of Health Medical Device Manufacturing No. 007177

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

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Produced in Taiwan, China

Dates and Status

Aug 21, 2021

Aug 21, 2026