Taiwan FDA registration 8211c90c4203a680b033fffff69d6ab4
“EUFOTON” LASEmaR mini Diode Laser System
TW: “悠扶盾”二極體雷射儀
Taiwan·Risk Class 2·MD·EUFOTON S.R.L.·Registered Jun 19, 2023 – Jun 19, 2028ActiveRegistration details
- Analysis ID
- 8211c90c4203a680b033fffff69d6ab4
- License Form
- Ministry of Health Medical Device Import No. 036546
- Customs Code
- DHA05603654606
Company information
- Manufacturer
- EUFOTON S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- Glory Group medical Co., Ltd.
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
- Jun 19, 2023
- Expiry Date
- Jun 19, 2028
About this record
Access comprehensive regulatory information for “EUFOTON” LASEmaR mini Diode 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 8211c90c4203a680b033fffff69d6ab4 and manufactured by EUFOTON S.R.L.. The authorized representative in Taiwan is Glory Group medical Co., Ltd..
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