Taiwan FDA registration ef6a4f7bfa5d6d33a2d3611ab2e21bc6
"Lominnis" lightteng pulsed light / laser and its accessories
TW: “洛明尼斯”光騰脈衝光/ 雷射儀及其配件
Taiwan·Risk Class 2·LUMENIS LTD.·Registered Jan 16, 2009 – Jan 16, 2019CancelledRegistration details
- Analysis ID
- ef6a4f7bfa5d6d33a2d3611ab2e21bc6
- Customs Code
- DHA00601956405
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- LUMENIS (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, 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 16, 2009
- Expiry Date
- Jan 16, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lominnis" lightteng pulsed light / laser and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ef6a4f7bfa5d6d33a2d3611ab2e21bc6 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is LUMENIS (HK) LIMITED TAIWAN BRANCH.
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