Taiwan FDA registration dfc261ebef64ebd5a5678d967c7c1126
“Lumenis” Array LaserLink Delivery Device
TW: “洛明尼斯”雷射傳輸系統
Taiwan·Risk Class 2·MD·LUMENIS INC.·Registered Dec 22, 2014 – Dec 22, 2024ExpiredRegistration details
- Analysis ID
- dfc261ebef64ebd5a5678d967c7c1126
- License Form
- Ministry of Health Medical Device Import No. 026912
- Customs Code
- DHA05602691202
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 Ophthalmic devices
- Product Type (Level 2)
- M4390 Ophthalmic laser unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2014
- Expiry Date
- Dec 22, 2024
About this record
Access comprehensive regulatory information for “Lumenis” Array LaserLink Delivery Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dfc261ebef64ebd5a5678d967c7c1126 and manufactured by LUMENIS INC.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.
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