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“Lumenis” Array LaserLink Delivery Device - Taiwan Registration dfc261ebef64ebd5a5678d967c7c1126

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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dfc261ebef64ebd5a5678d967c7c1126
Registration Details
Taiwan FDA Registration: dfc261ebef64ebd5a5678d967c7c1126
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Device Details

“Lumenis” Array LaserLink Delivery Device
TW: “洛明尼斯”雷射傳輸系統
Risk Class 2
MD

Registration Details

dfc261ebef64ebd5a5678d967c7c1126

Ministry of Health Medical Device Import No. 026912

DHA05602691202

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M4390 Ophthalmic laser unit

Imported from abroad

Dates and Status

Dec 22, 2014

Dec 22, 2024