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“NIDEK” Ophthalmic YAG Laser System - Taiwan Registration 50096fdc35785481ec6a6493c1af9e93

Access comprehensive regulatory information for “NIDEK” Ophthalmic YAG 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 50096fdc35785481ec6a6493c1af9e93 and manufactured by NIDEK CO., LTD. HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

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50096fdc35785481ec6a6493c1af9e93
Registration Details
Taiwan FDA Registration: 50096fdc35785481ec6a6493c1af9e93
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Device Details

“NIDEK” Ophthalmic YAG Laser System
TW: “尼德克”眼科雅各雷射系統
Risk Class 2
MD

Registration Details

50096fdc35785481ec6a6493c1af9e93

Ministry of Health Medical Device Import No. 032888

DHA05603288801

Company Information

Product Details

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

M Ophthalmic devices

M4392 Posterior capsulectomy with Nd:YAG laser

Imported from abroad

Dates and Status

Oct 04, 2019

Oct 04, 2024