Taiwan FDA registration f12e8d2b6a6bcc004f12af74983c9d96
"Sharp Light" pulsed light system
TW: “銳光”脈衝光系統
Taiwan·Risk Class 2·SHARPLIGHT TECHNOLOGIES LTD.·Registered Mar 12, 2008 – Mar 12, 2018CancelledRegistration details
- Analysis ID
- f12e8d2b6a6bcc004f12af74983c9d96
- Customs Code
- DHA00601863803
Company information
- Manufacturer
- SHARPLIGHT TECHNOLOGIES LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- Dongzhe Riki Medical 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
- import
Dates and status
- Registration Date
- Mar 12, 2008
- Expiry Date
- Mar 12, 2018
- Cancellation Date
- Feb 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 註銷藥商許可執照
About this record
Access comprehensive regulatory information for "Sharp Light" 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 f12e8d2b6a6bcc004f12af74983c9d96 and manufactured by SHARPLIGHT TECHNOLOGIES LTD.. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.
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