Taiwan FDA registration 5af57a9ccabf55abe4279e17b98ac554
"Euforten" medical diode laser
TW: “優芙特恩”醫用二極體雷射儀
Taiwan·Risk Class 2·EUFOTON S.R.L.·Registered Apr 02, 2015 – Apr 13, 2015CancelledRegistration details
- Analysis ID
- 5af57a9ccabf55abe4279e17b98ac554
- Customs Code
- DHA00602090607
Company information
- Manufacturer
- EUFOTON S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- QUANG-YANG 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
- Apr 02, 2015
- Expiry Date
- Apr 13, 2015
- Cancellation Date
- Feb 17, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Euforten" 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 5af57a9ccabf55abe4279e17b98ac554 and manufactured by EUFOTON S.R.L.. The authorized representative in Taiwan is QUANG-YANG CORPORATION.
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