Taiwan FDA registration 3b5e2f0b88505de61b3d1210c06cfffb
"Kentila" pulsed dye laser system
TW: "肯第拉"脈衝染料雷射系統
Taiwan·Risk Class 2·Valtronic Technologies (Suisse) SA;; Candela Corporation·Registered Jun 23, 2006 – Jun 23, 2026ExpiredRegistration details
- Analysis ID
- 3b5e2f0b88505de61b3d1210c06cfffb
- Customs Code
- DHA00601672909
Company information
- Manufacturer Country
- United States;;Switzerland
- 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
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jun 23, 2006
- Expiry Date
- Jun 23, 2026
About this record
Access comprehensive regulatory information for "Kentila" pulsed dye 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 3b5e2f0b88505de61b3d1210c06cfffb and manufactured by Valtronic Technologies (Suisse) SA;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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