Taiwan FDA registration fea860eff7a12e57b5aa52fb628f1a54
"Kentila" Alexander Laser
TW: "肯第拉 "亞歷山大雷射
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Jun 28, 1999 – Nov 04, 2016CancelledRegistration details
- Analysis ID
- fea860eff7a12e57b5aa52fb628f1a54
- Customs Code
- DHA00600922006
Company information
- Manufacturer
- CANDELA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
Product details
- Product Type (Level 1)
- 2199 Other medical laser devices
- Import Information
- import
Dates and status
- Registration Date
- Jun 28, 1999
- Expiry Date
- Nov 04, 2016
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentila" Alexander Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fea860eff7a12e57b5aa52fb628f1a54 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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