Taiwan FDA registration 43ec7f7c331291777460341a31a79e92

Funcare TENS/EMS

TW: 船井關健低周波治療器

Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Aug 24, 2020 – Aug 24, 2025Expired

Registration details

Analysis ID: 43ec7f7c331291777460341a31a79e92
License Form: Ministry of Health Medical Device Manufacturing No. 006957

Company information

Manufacturer: ASTEK TECHNOLOGY LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: ASTEK TECHNOLOGY LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5850 powered muscle stimulator
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 24, 2020
Expiry Date: Aug 24, 2025

About this record

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.