Taiwan FDA registration 8c8ece6676ed876ebfc08ce633e80546
"Kendela" picosecond neodymium Jacques laser system
TW: “肯得拉”皮秒衛釹雅克雷射系統
Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Nov 27, 2015 – Nov 27, 2025ExpiredRegistration details
- Analysis ID
- 8c8ece6676ed876ebfc08ce633e80546
- Customs Code
- DHA05602796206
Company information
- Manufacturer Country
- Mexico;;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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Nov 27, 2015
- Expiry Date
- Nov 27, 2025
About this record
Access comprehensive regulatory information for "Kendela" picosecond neodymium Jacques 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 8c8ece6676ed876ebfc08ce633e80546 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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