Taiwan FDA registration 695047b1588ea60de3edc0261ab0b636
"Kentila" diode laser system
TW: "肯第拉" 二極體雷射系統
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Apr 19, 2002 – Apr 19, 2022CancelledRegistration details
- Analysis ID
- 695047b1588ea60de3edc0261ab0b636
- Customs Code
- DHA00600988200
Company information
- Manufacturer
- CANDELA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- Apr 19, 2002
- Expiry Date
- Apr 19, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentila" diode 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 695047b1588ea60de3edc0261ab0b636 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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