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“Oculus” Scheimpflug Camera - Taiwan Registration f13adb951c52e87b679e315448e7f487

Access comprehensive regulatory information for “Oculus” Scheimpflug Camera in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f13adb951c52e87b679e315448e7f487 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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f13adb951c52e87b679e315448e7f487
Registration Details
Taiwan FDA Registration: f13adb951c52e87b679e315448e7f487
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Device Details

“Oculus” Scheimpflug Camera
TW: “歐克路”前房分析儀
Risk Class 2
MD

Registration Details

f13adb951c52e87b679e315448e7f487

Ministry of Health Medical Device Import No. 028778

DHA05602877805

Company Information

Germany

Product Details

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

M Ophthalmic devices

M1850 AC power type fine gap lamp

Imported from abroad

Dates and Status

Sep 02, 2016

Sep 02, 2026