Taiwan FDA registration 0129286c6fb82bf1519f80590a5fc415

funcare TENS

TW: 船井生醫低週波治療器
Taiwan flagTaiwan·Risk Class 2·MD·Hongtai Enterprise Co., Ltd. Rende Factory·Registered Oct 14, 2016 – Oct 14, 2026Active
Registration details
Analysis ID
0129286c6fb82bf1519f80590a5fc415
License Form
Ministry of Health Medical Device Manufacturing No. 005457
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 Devices for neuroscience
Product Type (Level 2)
K5890 Transcutaneous electrical nerve stimulator for pain relief
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Oct 14, 2016
Expiry Date
Oct 14, 2026
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About this record

Access comprehensive regulatory information for funcare TENS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0129286c6fb82bf1519f80590a5fc415 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 ASTEK TECHNOLOGY LTD., 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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