Taiwan FDA registration 41093d2312f9b4155057327d1eb73c4a
"Jingxuan" phototherapy instrument
TW: “敬煇”光療儀
Taiwan·Risk Class 2·TAIEX CO., LTD.·Registered Dec 28, 2006 – Dec 28, 2011CancelledRegistration details
- Analysis ID
- 41093d2312f9b4155057327d1eb73c4a
- Customs Code
- DHY00500211101
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX CO., LTD.
Product details
- Intended Use
- 線用於治療痤瘡(青春痘)(ACNE).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 28, 2006
- Expiry Date
- Dec 28, 2011
- Cancellation Date
- Mar 14, 2012
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Jingxuan" phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41093d2312f9b4155057327d1eb73c4a and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX CO., LTD..
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