"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.
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43b88047ac22559671e5091834fae565
Registration Details
Taiwan FDA Registration: 43b88047ac22559671e5091834fae565
Device Details
"Unilux" electrotherapy device
TW: โๅชๅ่ๆดปโ้ป็ๅจ
Risk Class 2

