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"Oculus" Keratograph (non-sterile) - Taiwan Registration 449dcb95434fd939d88a0761ef60bb9d

Access comprehensive regulatory information for "Oculus" Keratograph (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 449dcb95434fd939d88a0761ef60bb9d and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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449dcb95434fd939d88a0761ef60bb9d
Registration Details
Taiwan FDA Registration: 449dcb95434fd939d88a0761ef60bb9d
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Device Details

"Oculus" Keratograph (non-sterile)
TW: "ๆญๅฏๆจ‚ๆ–ฏ" ็œผ็ง‘่ง’่†œๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

449dcb95434fd939d88a0761ef60bb9d

Ministry of Health Medical Device Import Registration No. 004483

DHA08400448304

Company Information

Germany

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026