Taiwan FDA registration 3706a80fae533a5d902f977cb134628b
"Deca" Ritach diode laser system
TW: “狄卡”瑞塔奇二極體雷射系統
Taiwan·Risk Class 2·EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.·Registered Sep 07, 2022 – Sep 07, 2027ActiveRegistration details
- Analysis ID
- 3706a80fae533a5d902f977cb134628b
- Customs Code
- DHA05603580308
Company information
- Manufacturer
- EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- This product is a 675nm diode laser system for the treatment of benign pigmented lesions, acne scars and improvement of skin wrinkles.
- 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
- Sep 07, 2022
- Expiry Date
- Sep 07, 2027
About this record
Access comprehensive regulatory information for "Deca" Ritach diode 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 3706a80fae533a5d902f977cb134628b and manufactured by EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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