Khanma far-infrared therapy device - Taiwan Registration 72ca57f99cf0ff5229ab7056c4434648
Access comprehensive regulatory information for Khanma far-infrared 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 72ca57f99cf0ff5229ab7056c4434648 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is YI JIA GUO JI 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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72ca57f99cf0ff5229ab7056c4434648
Registration Details
Taiwan FDA Registration: 72ca57f99cf0ff5229ab7056c4434648
Device Details
Khanma far-infrared therapy device
TW: ๆฑ้ฆฌ้ ็ด
ๅค็ทๆฒป็ๅ
Risk Class 2

