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"Oculus" Ophthalmic trial lens set (non-sterile) - Taiwan Registration 57e42ae626e61bb22e92dba79d1b8521

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 57e42ae626e61bb22e92dba79d1b8521 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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57e42ae626e61bb22e92dba79d1b8521
Registration Details
Taiwan FDA Registration: 57e42ae626e61bb22e92dba79d1b8521
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Device Details

"Oculus" Ophthalmic trial lens set (non-sterile)
TW: "ๆญๅฏๆจ‚ๆ–ฏ" ็œผ็ง‘่ฉฆ้ฉ—้ก็‰‡็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

57e42ae626e61bb22e92dba79d1b8521

Ministry of Health Medical Device Import No. 017641

DHA09401764100

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

Mar 24, 2017

Mar 24, 2022