Taiwan FDA registration bad5991f59a4c4e48311e70f2976a39c
"Sero Xiu" Xinle Qi laser
TW: “色若修”欣樂綺雷射
Taiwan·Risk Class 2·CYNOSURE, LLC·Registered Jan 05, 2009 – Jan 05, 2029ActiveRegistration details
- Analysis ID
- bad5991f59a4c4e48311e70f2976a39c
- Customs Code
- DHA00601954807
Company information
- Manufacturer
- CYNOSURE, LLC
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- Jan 05, 2009
- Expiry Date
- Jan 05, 2029
About this record
Access comprehensive regulatory information for "Sero Xiu" Xinle Qi laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bad5991f59a4c4e48311e70f2976a39c and manufactured by CYNOSURE, LLC. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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