Taiwan FDA registration be2de80886408665d9e8c6fd32d4a73a
"Kentila" Q switches Alexandria laser system
TW: “肯第拉”Q開關亞歷山大雷射系統
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Apr 24, 2008 – Apr 24, 2023ExpiredRegistration details
- Analysis ID
- be2de80886408665d9e8c6fd32d4a73a
- Customs Code
- DHA00601882301
Company information
- Manufacturer
- CANDELA CORPORATION
- 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
- import
Dates and status
- Registration Date
- Apr 24, 2008
- Expiry Date
- Apr 24, 2023
About this record
Access comprehensive regulatory information for "Kentila" Q switches Alexandria 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 be2de80886408665d9e8c6fd32d4a73a and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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