Pure Global

"Unilux" electrotherapy device - Taiwan Registration 43b88047ac22559671e5091834fae565

Access comprehensive regulatory information for "Unilux" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43b88047ac22559671e5091834fae565 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is Jinli Health Technology Co., 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
43b88047ac22559671e5091834fae565
Registration Details
Taiwan FDA Registration: 43b88047ac22559671e5091834fae565
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Unilux" electrotherapy device
TW: โ€œๅ„ชๅŠ›่ˆ’ๆดปโ€้›ป็™‚ๅ™จ
Risk Class 2

Registration Details

43b88047ac22559671e5091834fae565

Company Information

Taiwan, Province of China

Product Details

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

o Physical Medical Sciences

O.5850 5850.

Contract manufacturing;; Domestic

Dates and Status

Jul 16, 2019

Mar 08, 2027