Taiwan FDA registration 55ab3b4851adb6d780543dd08a5f4f23
“Eufoton” LASEmar Laser
TW: “優芙登”雷射儀
Taiwan·Risk Class 2·MD·EUFOTON S.r.l.·Registered Nov 16, 2016 – Nov 16, 2021CancelledRegistration details
- Analysis ID
- 55ab3b4851adb6d780543dd08a5f4f23
- License Form
- Ministry of Health Medical Device Import No. 029053
- Customs Code
- DHA05602905305
Company information
- Manufacturer
- EUFOTON S.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- WAY SEEN INTERNATIONAL CO., LTD.
Product details
- 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
- Nov 16, 2016
- Expiry Date
- Nov 16, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Eufoton” LASEmar Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55ab3b4851adb6d780543dd08a5f4f23 and manufactured by EUFOTON S.r.l.. The authorized representative in Taiwan is WAY SEEN INTERNATIONAL CO., LTD..
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