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“OCULUS” Ophthalmic Trial Lens Set (Non-Sterile) - Taiwan Registration 585f52494ed02035aebf175040a3a802

Access comprehensive regulatory information for “OCULUS” Ophthalmic Trial Lens Set (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 585f52494ed02035aebf175040a3a802 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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585f52494ed02035aebf175040a3a802
Registration Details
Taiwan FDA Registration: 585f52494ed02035aebf175040a3a802
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Device Details

“OCULUS” Ophthalmic Trial Lens Set (Non-Sterile)
TW: “歐克勒斯”眼科試驗鏡片組 (未滅菌)
Risk Class 1
MD

Registration Details

585f52494ed02035aebf175040a3a802

Ministry of Health Medical Device Import No. 021074

DHA09402107406

Company Information

Germany

Product Details

Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1405 Ophthalmic Test Lens Group

Imported from abroad

Dates and Status

Dec 05, 2019

Dec 05, 2024