Taiwan FDA registration 9b360cfaba2c811881fc430d620e2956
“Lumenis” ResurFx Laser System
TW: “洛明尼斯”梭時雷射系統
Taiwan·Risk Class 2·MD·LUMENIS LTD.·Registered Jul 19, 2016 – Jul 19, 2026ExpiredRegistration details
- Analysis ID
- 9b360cfaba2c811881fc430d620e2956
- License Form
- Ministry of Health Medical Device Import No. 028634
- Customs Code
- DHA05602863407
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 19, 2016
- Expiry Date
- Jul 19, 2026
About this record
Access comprehensive regulatory information for “Lumenis” ResurFx 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 9b360cfaba2c811881fc430d620e2956 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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