Taiwan FDA registration 72ca57f99cf0ff5229ab7056c4434648
Khanma far-infrared therapy device
TW: 汗馬遠紅外線治療儀
Taiwan·Risk Class 2·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered May 26, 2014 – May 26, 2029ActiveRegistration details
- Analysis ID
- 72ca57f99cf0ff5229ab7056c4434648
Company information
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YI JIA GUO JI CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5500 Infrared lamp
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- May 26, 2014
- Expiry Date
- May 26, 2029
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices