Taiwan FDA registration 6115442ba2b1950e3bf204378b1a204a
"Liverage" Laser treatment instrument
TW: "千才" 雷射治療儀
Taiwan·Risk Class 2·MD·LIVERAGE TECHNOLOGY INC.·Registered Nov 01, 2017 – Nov 01, 2027ActiveRegistration details
- Analysis ID
- 6115442ba2b1950e3bf204378b1a204a
- License Form
- Ministry of Health Medical Device Manufacturing No. 005921
Company information
- Manufacturer
- LIVERAGE TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LIVERAGE BIOMEDICAL INC.
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 01, 2017
- Expiry Date
- Nov 01, 2027
About this record
Access comprehensive regulatory information for "Liverage" Laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6115442ba2b1950e3bf204378b1a204a and manufactured by LIVERAGE TECHNOLOGY INC.. The authorized representative in Taiwan is LIVERAGE BIOMEDICAL INC..
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