Taiwan FDA registration 3880dacdcb94365945d7496fa7b2aca5
"DORNIER" medical holmium laser treatment instrument
TW: "多尼爾"醫用鈥雷射治療儀
Taiwan·Risk Class 2·DORNIER MEDTECH SYSTEMS GMBH·Registered Jul 10, 2006 – Jul 10, 2021CancelledRegistration details
- Analysis ID
- 3880dacdcb94365945d7496fa7b2aca5
- Customs Code
- DHA00601685705
Company information
- Manufacturer
- DORNIER MEDTECH SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN INTERNATIONAL 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
- Jul 10, 2006
- Expiry Date
- Jul 10, 2021
- Cancellation Date
- Aug 09, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "DORNIER" medical holmium 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 3880dacdcb94365945d7496fa7b2aca5 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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