Pure Global

"Nidek" corneal lamellar knife (unsterilized) - Taiwan Registration 368697082e87e528f632ece58b17c468

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 368697082e87e528f632ece58b17c468 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
368697082e87e528f632ece58b17c468
Registration Details
Taiwan FDA Registration: 368697082e87e528f632ece58b17c468
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

368697082e87e528f632ece58b17c468

DHA04401066206

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

Aug 01, 2011

Aug 01, 2016

Apr 13, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ