Taiwan FDA registration 9da737cb8f7532b4c3ea710f00774433
"Uverton" medical diode laser
TW: “優弗頓”醫用二極體雷射儀
Taiwan·Risk Class 2·EUFOTON S.R.L.·Registered Oct 26, 2012 – Oct 26, 2027ActiveRegistration details
- Analysis ID
- 9da737cb8f7532b4c3ea710f00774433
- Customs Code
- DHA00602407102
Company information
- Manufacturer
- EUFOTON S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- WAY SEEN INTERNATIONAL CO., LTD.
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
- Oct 26, 2012
- Expiry Date
- Oct 26, 2027
About this record
Access comprehensive regulatory information for "Uverton" medical diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9da737cb8f7532b4c3ea710f00774433 and manufactured by EUFOTON S.R.L.. The authorized representative in Taiwan is WAY SEEN INTERNATIONAL CO., LTD..
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