Taiwan FDA registration 11dbfc1fe134a4af2007a87821574c33
"Daxin" pulsed light system
TW: “大新”脈衝光系統
Taiwan·Risk Class 2·DAESHIN ENTERPRISE·Registered Jan 16, 2008 – Jan 16, 2018CancelledRegistration details
- Analysis ID
- 11dbfc1fe134a4af2007a87821574c33
- Customs Code
- DHA00601854509
Company information
- Manufacturer
- DAESHIN ENTERPRISE
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PIEZOMED INTERNATIONAL INC.
Product details
- Intended Use
- Treatment of pigmented lesions, vascular lesions, and hair removal.
- 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
- Jan 16, 2008
- Expiry Date
- Jan 16, 2018
- Cancellation Date
- Nov 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Daxin" pulsed light system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11dbfc1fe134a4af2007a87821574c33 and manufactured by DAESHIN ENTERPRISE. The authorized representative in Taiwan is PIEZOMED INTERNATIONAL INC..
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