Taiwan FDA registration 4f2cc1ad6eb479641062e38a64978b0e
“Cynosure” Cellulaze Laser System
TW: “色若修”色露蕾絲雷射儀
Taiwan·Risk Class 2·MD·CYNOSURE, LLC·Registered Jan 22, 2014 – Jan 22, 2024ExpiredRegistration details
- Analysis ID
- 4f2cc1ad6eb479641062e38a64978b0e
- License Form
- Ministry of Health Medical Device Import No. 025349
- Customs Code
- DHA05602534906
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 and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 22, 2014
- Expiry Date
- Jan 22, 2024
About this record
Access comprehensive regulatory information for “Cynosure” Cellulaze 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 4f2cc1ad6eb479641062e38a64978b0e and manufactured by CYNOSURE, LLC. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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