Taiwan FDA registration 31aee288671ab218471e4db92fb8816d
"Kudra" Inleiden picosecond laser system
TW: “酷德拉”因萊頓皮秒雷射系統
Taiwan·Risk Class 2·CUTERA, INC.·Registered Mar 22, 2016 – Mar 22, 2026ExpiredRegistration details
- Analysis ID
- 31aee288671ab218471e4db92fb8816d
- Customs Code
- DHA05602834003
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
- Mar 22, 2016
- Expiry Date
- Mar 22, 2026
About this record
Access comprehensive regulatory information for "Kudra" Inleiden picosecond 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 31aee288671ab218471e4db92fb8816d and manufactured by CUTERA, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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