Taiwan FDA registration 520100f627f89b78a856449cd29ef5c1

"Jetway" phototherapy instrument

TW: “捷威”光療儀

Taiwan·Risk Class 2·MESURE TECHNOLOGY CO., LTD.·Registered Apr 20, 2007 – Apr 20, 2022Cancelled

Registration details

Analysis ID: 520100f627f89b78a856449cd29ef5c1
Customs Code: DHY00500219102

Company information

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

Product details

Intended Use: Restricted to the treatment of acne (acne) (ACNE).
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: Apr 20, 2007
Expiry Date: Apr 20, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Jetway" 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 520100f627f89b78a856449cd29ef5c1 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.