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"Sight Wonder" corneal knife (unsterilized) - Taiwan Registration 1b2ab5b40e01896f1876881678f5ef5f

Access comprehensive regulatory information for "Sight Wonder" corneal knife (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b2ab5b40e01896f1876881678f5ef5f and manufactured by SCHWIND EYE-TECH-SOLUTIONS GMBH. 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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1b2ab5b40e01896f1876881678f5ef5f
Registration Details
Taiwan FDA Registration: 1b2ab5b40e01896f1876881678f5ef5f
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Device Details

"Sight Wonder" corneal knife (unsterilized)
TW: "่ฆ–่ฌๅพ—" ่ง’่†œๅˆ€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1b2ab5b40e01896f1876881678f5ef5f

DHA04400930406

Company Information

Product Details

Limited to the first level identification range of the "corneal knife (M.4370)" of the Measures for the Administration of Medical Devices.

M Ophthalmology

M.4370 Corneal knife

import

Dates and Status

Oct 04, 2010

Oct 04, 2020

Aug 05, 2022

Cancellation Information

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