Taiwan FDA registration d1ddf7cf2af8f22f4fe9cb6edafe54a8
"Kentila" Proalexander's laser system
TW: “肯第拉”普若亞歷山大雷射系統
Taiwan·Risk Class 2·CANDELA CORPORATION·Registered Mar 13, 2012 – Mar 13, 2027ActiveRegistration details
- Analysis ID
- d1ddf7cf2af8f22f4fe9cb6edafe54a8
- Customs Code
- DHA00602337402
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Mar 13, 2012
- Expiry Date
- Mar 13, 2027
About this record
Access comprehensive regulatory information for "Kentila" Proalexander's 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 d1ddf7cf2af8f22f4fe9cb6edafe54a8 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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