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“ESSILOR” Trial Frame (Non-Sterile) - Taiwan Registration 874c0d94d453f8804a71e5dd8558a84f

Access comprehensive regulatory information for “ESSILOR” Trial Frame (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 874c0d94d453f8804a71e5dd8558a84f and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

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874c0d94d453f8804a71e5dd8558a84f
Registration Details
Taiwan FDA Registration: 874c0d94d453f8804a71e5dd8558a84f
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Device Details

“ESSILOR” Trial Frame (Non-Sterile)
TW: “依視路” 試驗鏡片夾 (未滅菌)
Risk Class 1
MD

Registration Details

874c0d94d453f8804a71e5dd8558a84f

Ministry of Health Medical Device Import No. 021668

DHA09402166809

Company Information

Germany

Product Details

Limited to the first level recognition range of the ophthalmic test lens clip (M.1410) of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1410 Lens clip for ophthalmic test

Imported from abroad

Dates and Status

Jun 24, 2020

Jun 24, 2025