Taiwan FDA registration ea2ea4d23c8759f13b6dcd3144a1d2fa

"Kentila" Pro laser system

TW: “肯第拉”普若雷射系統

Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Oct 02, 2013 – Oct 02, 2028Active

Registration details

Analysis ID: ea2ea4d23c8759f13b6dcd3144a1d2fa
Customs Code: DHA05602548300

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: Contract manufacturing;; input

Dates and status

Registration Date: Oct 02, 2013
Expiry Date: Oct 02, 2028

About this record

Access comprehensive regulatory information for "Kentila" Pro 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 ea2ea4d23c8759f13b6dcd3144a1d2fa 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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