Taiwan FDA registration 5524f67ea2fb66aedefe8ea0a9db6d82
"Kendela" Flying Shuttle laser system
TW: “肯得拉”飛波飛梭雷射系統
Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Aug 21, 2023 – Oct 02, 2028ActiveRegistration details
- Analysis ID
- 5524f67ea2fb66aedefe8ea0a9db6d82
- Customs Code
- DHA05603165907
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;; 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
- Aug 21, 2023
- Expiry Date
- Oct 02, 2028
About this record
Access comprehensive regulatory information for "Kendela" Flying Shuttle 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 5524f67ea2fb66aedefe8ea0a9db6d82 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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices