Taiwan FDA registration e8246a7c8f9a065f141ac66f6d3d4490
"Kentila" Ress laser system
TW: “肯第拉”雷斯雷射系統
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Sep 16, 2008 – Sep 16, 2023ExpiredRegistration details
- Analysis ID
- e8246a7c8f9a065f141ac66f6d3d4490
- Customs Code
- DHA00601921200
Company information
- Manufacturer
- CANDELA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
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
- Sep 16, 2008
- Expiry Date
- Sep 16, 2023
About this record
Access comprehensive regulatory information for "Kentila" Ress 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 e8246a7c8f9a065f141ac66f6d3d4490 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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