Taiwan FDA registration 79f812348889b569c4fd15a04e1f9690
"Lominnis" WiseVision Green Laser System and its accessories
TW: “洛明尼斯”慧視能綠雷射系統及其附件
Taiwan·Risk Class 2·Lumenis Be Inc.·Registered Jul 13, 2017 – Jul 13, 2027ActiveRegistration details
- Analysis ID
- 79f812348889b569c4fd15a04e1f9690
- Customs Code
- DHA05602996802
Company information
- Manufacturer
- Lumenis Be 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
- Jul 13, 2017
- Expiry Date
- Jul 13, 2027
About this record
Access comprehensive regulatory information for "Lominnis" WiseVision Green Laser System 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 79f812348889b569c4fd15a04e1f9690 and manufactured by Lumenis Be Inc.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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