Taiwan FDA registration bad18a4e69b14343ec491558ddd5417a
“CUTERA” enlighten Laser System
TW: “奎特拉”茵萊敦雷射系統
Taiwan·Risk Class 2·MD·CUTERA, INC.·Registered Dec 29, 2015 – Dec 29, 2025ExpiredRegistration details
- Analysis ID
- bad18a4e69b14343ec491558ddd5417a
- License Form
- Ministry of Health Medical Device Import No. 028032
- Customs Code
- DHA05602803205
Company information
- Manufacturer
- CUTERA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Dec 29, 2015
- Expiry Date
- Dec 29, 2025
About this record
Access comprehensive regulatory information for “CUTERA” enlighten 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 bad18a4e69b14343ec491558ddd5417a and manufactured by CUTERA, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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