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Nidek corneal lamellar knife (unsterilized) - Taiwan Registration fc00b2d21a37768d2b9e378af258d81e

Access comprehensive regulatory information for Nidek corneal lamellar 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 fc00b2d21a37768d2b9e378af258d81e 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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fc00b2d21a37768d2b9e378af258d81e
Registration Details
Taiwan FDA Registration: fc00b2d21a37768d2b9e378af258d81e
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Device Details

Nidek corneal lamellar knife (unsterilized)
TW: ๅฐผๅพทๅ…‹่ง’่†œๆฟๅฑคๅˆ€(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fc00b2d21a37768d2b9e378af258d81e

DHA04400283706

Company Information

Japan

Product Details

A keratoblade is an alternating current or battery-powered device used to trim tissues during corneal lamellar transplantation (cornea of partial thickness).

M Ophthalmology

M.4370 Corneal knife

import

Dates and Status

Mar 08, 2006

Mar 08, 2011

Jan 21, 2013

Cancellation Information

Logged out

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