Taiwan FDA registration 27621cfe969ffc0f9ce930a166752554
"New Nalon" e laser system
TW: "新那隆"e雷射系統
Taiwan·Risk Class 2·SYNERON MEDICAL LTD.·Registered Dec 28, 2006 – Dec 28, 2016CancelledRegistration details
- Analysis ID
- 27621cfe969ffc0f9ce930a166752554
- Customs Code
- DHA00601763900
Company information
- Manufacturer
- SYNERON MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- LYRA 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
- Dec 28, 2006
- Expiry Date
- Dec 28, 2016
- Cancellation Date
- Aug 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "New Nalon" e laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27621cfe969ffc0f9ce930a166752554 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is LYRA LTD..
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