Taiwan FDA registration 0b79733f5fd9557c5aa9e85d1de14417
"New Nalon" medical light pulse system
TW: "新那隆"醫光脈衝系統
Taiwan·Risk Class 2·SYNERON MEDICAL LTD.·Registered Jan 24, 2007 – Jan 24, 2017CancelledRegistration details
- Analysis ID
- 0b79733f5fd9557c5aa9e85d1de14417
- Customs Code
- DHA00601772009
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- LYRA LTD.
Product details
- Intended Use
- For details, please refer to the approved version of Chinese copy
- 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 24, 2007
- Expiry Date
- Jan 24, 2017
- Cancellation Date
- Dec 13, 2019
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 light pulse system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b79733f5fd9557c5aa9e85d1de14417 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is LYRA LTD..
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