Taiwan FDA registration fd6f8aaaa7b004c7783543b8b1d6821c
"Lominnis" Viyi eye laser system
TW: “洛明尼斯”維依眼用雷射系統
Taiwan·Risk Class 2·LUMENIS INC.·Registered Nov 07, 2012 – Nov 07, 2022CancelledRegistration details
- Analysis ID
- fd6f8aaaa7b004c7783543b8b1d6821c
- Customs Code
- DHA00602418606
Company information
- Manufacturer
- LUMENIS INC.
- Manufacturer Country
- United States
- 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)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2012
- Expiry Date
- Nov 07, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lominnis" Viyi eye 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 fd6f8aaaa7b004c7783543b8b1d6821c and manufactured by LUMENIS INC.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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