Taiwan FDA registration 27432d77f1f348eba5aa2b7021c1e8a0

"Jetway" wound phototherapy instrument

TW: “捷威”傷口光療儀

Taiwan·Risk Class 2·MESURE TECHNOLOGY CO., LTD.·Registered Aug 26, 2008 – Aug 26, 2023Expired

Registration details

Analysis ID: 27432d77f1f348eba5aa2b7021c1e8a0
Customs Code: DHY00500249404

Company information

Manufacturer: MESURE TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: MESURE TECHNOLOGY CO., LTD.

Product details

Intended Use: To promote wound healing, this product should be prescribed by a physician.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information: Domestic

Dates and status

Registration Date: Aug 26, 2008
Expiry Date: Aug 26, 2023

About this record

Access comprehensive regulatory information for "Jetway" wound phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27432d77f1f348eba5aa2b7021c1e8a0 and manufactured by MESURE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is MESURE 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.