Taiwan FDA registration 029de274f6664ddcbd1e93ecee50e1c9
"Lomenis" glaucoma laser
TW: “洛明尼斯”青光眼雷射儀
Taiwan·Risk Class 2·LUMENIS, INC.·Registered Mar 29, 2007 – Mar 29, 2012CancelledRegistration details
- Analysis ID
- 029de274f6664ddcbd1e93ecee50e1c9
- Customs Code
- DHA00601796908
Company information
- Manufacturer
- LUMENIS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHIU HO MEDICAL SYSTEM 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
- Mar 29, 2007
- Expiry Date
- Mar 29, 2012
- Cancellation Date
- Apr 16, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lomenis" 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 029de274f6664ddcbd1e93ecee50e1c9 and manufactured by LUMENIS, INC.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..
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