Taiwan FDA registration 7f4b715eebafae356b560612f4e3a041

"Funai" low week wave therapy device

TW: “船井”低週波治療器
Taiwan flagTaiwan·Risk Class 2·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Oct 16, 2020 – Oct 16, 2025Expired
Registration details
Analysis ID
7f4b715eebafae356b560612f4e3a041
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Neuroscience;;O Physical Medical Sciences
Product Type (Level 2)
K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
Import Information
Domestic
Dates and status
Registration Date
Oct 16, 2020
Expiry Date
Oct 16, 2025
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About this record

Access comprehensive regulatory information for "Funai" low week wave 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 7f4b715eebafae356b560612f4e3a041 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is Hongtai Enterprise Co., Ltd. Rende Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hongtai Enterprise Co., Ltd. Rende Factory, and 1 recent registrations in the same category. 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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