Taiwan FDA registration e776d468e2bcd934d0bcb99e591ea6a9
"Lominnis" Celite glaucoma laser
TW: “洛明尼斯”色麗特青光眼雷射儀
Taiwan·Risk Class 2·LUMENIS, INC.·Registered Jul 21, 2009 – Jul 21, 2014CancelledRegistration details
- Analysis ID
- e776d468e2bcd934d0bcb99e591ea6a9
- Customs Code
- DHA00602007200
Company information
- Manufacturer
- LUMENIS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Branch of Hong Kong Commercial Medical Laser Co., 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
- Jul 21, 2009
- Expiry Date
- Jul 21, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lominnis" Celite glaucoma laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e776d468e2bcd934d0bcb99e591ea6a9 and manufactured by LUMENIS, INC.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Medical Laser Co., Ltd.
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