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“OPTIKON”Keratron Corneal Topographer(Non-Sterile) - Taiwan Registration afe6f9d47e89b9f6a141324b37acb37f

Access comprehensive regulatory information for “OPTIKON”Keratron Corneal Topographer(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 afe6f9d47e89b9f6a141324b37acb37f and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is OPTACT INTERNATIONAL CO., LTD..

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afe6f9d47e89b9f6a141324b37acb37f
Registration Details
Taiwan FDA Registration: afe6f9d47e89b9f6a141324b37acb37f
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Device Details

“OPTIKON”Keratron Corneal Topographer(Non-Sterile)
TW: “奧蒂康”科瑞創角膜地圖儀(未滅菌)
Risk Class 1
MD

Registration Details

afe6f9d47e89b9f6a141324b37acb37f

Ministry of Health Medical Device Import Registration No. 010057

DHA08401005702

Company Information

Italy

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