Taiwan FDA registration 30de9c067425297b65919c7ca33fc9ef
“Candela” Vbeam Prima Laser System
TW: “肯得拉”光優染料雷射系統
Taiwan·Risk Class 2·MD·CANDELA CORPORATION·Registered Feb 03, 2020 – Feb 03, 2025ExpiredRegistration details
- Analysis ID
- 30de9c067425297b65919c7ca33fc9ef
- License Form
- Ministry of Health Medical Device Import No. 033182
- Customs Code
- DHA05603318205
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 and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 03, 2020
- Expiry Date
- Feb 03, 2025
About this record
Access comprehensive regulatory information for “Candela” Vbeam Prima 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 30de9c067425297b65919c7ca33fc9ef and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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