Taiwan FDA registration acc8f22609ca7ac67abb2d54433fc99b

"Kendela" aurora pulsed light and laser system

TW: “肯得拉”極光脈衝光及雷射系統

Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Nov 28, 2016 – Nov 28, 2026Active

Registration details

Analysis ID: acc8f22609ca7ac67abb2d54433fc99b
Customs Code: DHA05602908709

Company information

Manufacturer: NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation
Manufacturer Country: Mexico;;United States
Authorized Representative: DYNAMIC MEDICAL TECHNOLOGIES INC.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
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: Input;; The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Contract manufacturing

Dates and status

Registration Date: Nov 28, 2016
Expiry Date: Nov 28, 2026

About this record

Access comprehensive regulatory information for "Kendela" aurora pulsed light and laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number acc8f22609ca7ac67abb2d54433fc99b and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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.