Taiwan FDA registration ca99e49aa67c9c7b614d24bd25c27a5a
"Kendela" gentle Yak neodymium Jacques laser
TW: "肯得拉"溫和雅客釹雅克雷射
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Apr 28, 2005 – Apr 28, 2025ExpiredRegistration details
- Analysis ID
- ca99e49aa67c9c7b614d24bd25c27a5a
- Customs Code
- DHA00601123307
Company information
- Manufacturer
- CANDELA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- For details Chinese Approved copy of the copy is blanked below
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- Apr 28, 2005
- Expiry Date
- Apr 28, 2025
About this record
Access comprehensive regulatory information for "Kendela" gentle Yak neodymium Jacques laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca99e49aa67c9c7b614d24bd25c27a5a and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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