Taiwan FDA registration abe37d854a57d24cf978e09de2f28360
"New Nalon" medical dream pulsed light system
TW: “新那隆”醫夢脈衝光系統
Taiwan·Risk Class 2·SYNERON MEDICAL LTD.·Registered Oct 15, 2007 – Oct 15, 2012CancelledRegistration details
- Analysis ID
- abe37d854a57d24cf978e09de2f28360
- Customs Code
- DHA00601835902
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- Conservation Corporation Limited
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 15, 2007
- Expiry Date
- Oct 15, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "New Nalon" medical dream 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 abe37d854a57d24cf978e09de2f28360 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is Conservation Corporation Limited.
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