Taiwan FDA registration 3f720dc0d950f83c6aef210b07ca28b3
"Qiancai" laser therapy device accessories (single-use fiber optic needle)
TW: “千才”雷射治療儀附件(一次性使用光纖針)
Taiwan·Risk Class 2·LIVERAGE TECHNOLOGY INC.·Registered Aug 28, 2017 – Aug 28, 2027ActiveRegistration details
- Analysis ID
- 3f720dc0d950f83c6aef210b07ca28b3
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 28, 2017
- Expiry Date
- Aug 28, 2027
About this record
Access comprehensive regulatory information for "Qiancai" laser therapy device accessories (single-use fiber optic needle) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f720dc0d950f83c6aef210b07ca28b3 and manufactured by LIVERAGE TECHNOLOGY INC.. The authorized representative in Taiwan is LIVERAGE BIOMEDICAL INC..
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