Taiwan FDA registration f52fefdff1af2279f774839ca22bcd58

"Deca" Mortex laser

TW: “德卡”摩特絲雷射

Taiwan·Risk Class 2·DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.·Registered Sep 15, 2017 – Sep 15, 2027Active

Registration details

Analysis ID: f52fefdff1af2279f774839ca22bcd58
Customs Code: DHA05603023205

Company information

Manufacturer: DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.
Manufacturer Country: Italy
Authorized Representative: K&C MEDICAL CO., LTD.

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;; Contract manufacturing

Dates and status

Registration Date: Sep 15, 2017
Expiry Date: Sep 15, 2027

About this record

Access comprehensive regulatory information for "Deca" Mortex laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f52fefdff1af2279f774839ca22bcd58 and manufactured by DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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