"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.
Device Details
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
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