Taiwan FDA registration 89b7d6f2b25d8b9cdde18eac9278ac05

"Kudra" Inleidensl picosecond laser system and its accessories

TW: “酷德拉”因萊頓斯爾皮秒雷射系統及其配件

Taiwan·Risk Class 2·CUTERA, INC.·Registered Oct 08, 2018 – Oct 08, 2028Active

Registration details

Analysis ID: 89b7d6f2b25d8b9cdde18eac9278ac05
Customs Code: DHA05603166502

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: 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.

Dates and status

Registration Date: Oct 08, 2018
Expiry Date: Oct 08, 2028

About this record

Access comprehensive regulatory information for "Kudra" Inleidensl picosecond laser system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 89b7d6f2b25d8b9cdde18eac9278ac05 and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..

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