Taiwan FDA registration d702c1de94907dd1d53ab9cbf26d92f7
“Cynosure” Elite iQ Alexandrite and Nd:YAG Laser System and Accessories
TW: “色若修”亞歷山大及釹雅鉻雷射系統及其配件
Taiwan·Risk Class 2·MD·DEKA M.E.L.A. S.R.L.·Registered Jan 16, 2023 – Jan 16, 2028ActiveRegistration details
- Analysis ID
- d702c1de94907dd1d53ab9cbf26d92f7
- License Form
- Ministry of Health Medical Device Import No. 036284
- Customs Code
- DHA05603628402
Company information
- Manufacturer
- DEKA M.E.L.A. S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 16, 2023
- Expiry Date
- Jan 16, 2028
About this record
Access comprehensive regulatory information for “Cynosure” Elite iQ Alexandrite and Nd:YAG Laser System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d702c1de94907dd1d53ab9cbf26d92f7 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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