Taiwan FDA registration f56d9c3c77f20dd83c27cd6d7f75367f
"Medis" CO2 laser treatment instrument
TW: “麥迪斯”二氧化碳雷射治療儀
Taiwan·Risk Class 2·SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.·Registered Oct 06, 2008 – Oct 06, 2013CancelledRegistration details
- Analysis ID
- f56d9c3c77f20dd83c27cd6d7f75367f
- Customs Code
- DHA00601925505
Company information
- Manufacturer Country
- United States
- Authorized Representative
- LITE-MED 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
- import
Dates and status
- Registration Date
- Oct 06, 2008
- Expiry Date
- Oct 06, 2013
- Cancellation Date
- May 28, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medis" CO2 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 f56d9c3c77f20dd83c27cd6d7f75367f and manufactured by SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.. The authorized representative in Taiwan is LITE-MED INC..
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