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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
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Device Details

Khanma far-infrared therapy device
TW: ๆฑ—้ฆฌ้ ็ด…ๅค–็ทšๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

72ca57f99cf0ff5229ab7056c4434648

Company Information

Taiwan, Province of China

Product Details

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

o Physical Medical Sciences

O.5500 Infrared lamp

Contract manufacturing;; Domestic

Dates and Status

May 26, 2014

May 26, 2029