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"Nidek" corneal curvature - Taiwan Registration 9d1a8142aeae67ec26c59c2f50b2386a

Access comprehensive regulatory information for "Nidek" corneal curvature in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d1a8142aeae67ec26c59c2f50b2386a and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

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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9d1a8142aeae67ec26c59c2f50b2386a
Registration Details
Taiwan FDA Registration: 9d1a8142aeae67ec26c59c2f50b2386a
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Device Details

"Nidek" corneal curvature
TW: "ๅฐผๅพทๅ…‹" ่ง’่†œๅผงๅบฆๅ„€
Risk Class 1
Cancelled

Registration Details

9d1a8142aeae67ec26c59c2f50b2386a

DHA04400269502

Company Information

Japan

Product Details

It is an alternating current or battery-powered device used to measure and evaluate the curvature of the cornea of the eye. The lines and circles in the keratometer are used to observe the corneal reflex. The general type of device includes a photokeratometer, which can be used to record the curvature of the cornea using corneal photography.

M Ophthalmology

M.1350 Coratoscope

import

Dates and Status

Feb 22, 2006

Feb 22, 2011

Jan 21, 2013

Cancellation Information

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