Taiwan FDA registration 84cfb332453f860746fa64e9e47cfd5e
"Jingxuan" laser therapy instrument
TW: “敬煇”雷射治療儀
Taiwan·Risk Class 2·TAIEX CO., LTD.·Registered Feb 01, 2013 – Feb 01, 2028ActiveRegistration details
- Analysis ID
- 84cfb332453f860746fa64e9e47cfd5e
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX CO., LTD.
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
- Domestic
Dates and status
- Registration Date
- Feb 01, 2013
- Expiry Date
- Feb 01, 2028
About this record
Access comprehensive regulatory information for "Jingxuan" laser therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84cfb332453f860746fa64e9e47cfd5e and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..
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