Taiwan FDA registration 1d474bca2b8ccc98a8d5c1148d58e843
"Lomenis" ophthalmic laser device
TW: “洛明尼斯”眼科雷射裝置
Taiwan·Risk Class 2·LUMENIS INC.·Registered Jan 30, 2008 – Jan 30, 2013CancelledRegistration details
- Analysis ID
- 1d474bca2b8ccc98a8d5c1148d58e843
- Customs Code
- DHA00601857008
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)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Jan 30, 2008
- Expiry Date
- Jan 30, 2013
- Cancellation Date
- Apr 24, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lomenis" ophthalmic laser device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d474bca2b8ccc98a8d5c1148d58e843 and manufactured by LUMENIS INC.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..
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