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“Optovue” Keratoscope (Non-Sterile) - Taiwan Registration c45920374197b7f001ce3a3655569ac1

Access comprehensive regulatory information for “Optovue” Keratoscope (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 c45920374197b7f001ce3a3655569ac1 and manufactured by OPTOVUE INC.. The authorized representative in Taiwan is CLINICO INC..

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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c45920374197b7f001ce3a3655569ac1
Registration Details
Taiwan FDA Registration: c45920374197b7f001ce3a3655569ac1
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Device Details

“Optovue” Keratoscope (Non-Sterile)
TW: “歐威”角膜鏡(未滅菌)
Risk Class 1
MD

Registration Details

c45920374197b7f001ce3a3655569ac1

Ministry of Health Medical Device Import Registration No. 012136

DHA08401213605

Company Information

United States

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, 2023