Taiwan FDA registration 2868b79b48a2187dd4405c5745a27e6d

"Cooldra" Inleiden three-picosecond laser system and accessories

TW: “酷德拉”因萊頓叁皮秒雷射系統及其配件

Taiwan·Risk Class 2·CUTERA, INC.·Registered Mar 05, 2018 – Mar 05, 2028Active

Registration details

Analysis ID: 2868b79b48a2187dd4405c5745a27e6d
Customs Code: DHA05603094503

Company information

Manufacturer: CUTERA, INC.
Manufacturer Country: United States
Authorized Representative: AESOLUTION BIOMEDICAL 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: 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". input

Dates and status

Registration Date: Mar 05, 2018
Expiry Date: Mar 05, 2028

About this record

Access comprehensive regulatory information for "Cooldra" Inleiden three-picosecond laser system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2868b79b48a2187dd4405c5745a27e6d and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..

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