Taiwan FDA registration 6d0bbfd2585cb5d9e4e4c57b0416b253

"Kentila" Jutemax laser system

TW: “肯第拉”爵特麥斯雷射系統

Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Nov 08, 2016 – Nov 08, 2026Active

Registration details

Analysis ID: 6d0bbfd2585cb5d9e4e4c57b0416b253
Customs Code: DHA05602901803

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 08, 2016
Expiry Date: Nov 08, 2026

About this record

Access comprehensive regulatory information for "Kentila" Jutemax 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 6d0bbfd2585cb5d9e4e4c57b0416b253 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..

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