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Funcare TENS/EMS - Taiwan Registration 43ec7f7c331291777460341a31a79e92

Access comprehensive regulatory information for Funcare TENS/EMS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43ec7f7c331291777460341a31a79e92 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY LTD..

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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43ec7f7c331291777460341a31a79e92
Registration Details
Taiwan FDA Registration: 43ec7f7c331291777460341a31a79e92
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Device Details

Funcare TENS/EMS
TW: ่ˆนไบ•้—œๅฅไฝŽๅ‘จๆณขๆฒป็™‚ๅ™จ
Risk Class 2
MD

Registration Details

43ec7f7c331291777460341a31a79e92

Ministry of Health Medical Device Manufacturing No. 006957

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

o Equipment for physical medicine

O5850 powered muscle stimulator

Produced in Taiwan, China

Dates and Status

Aug 24, 2020

Aug 24, 2025