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"Nidek" corneal mapper (unsterilized) - Taiwan Registration 9e6a5f2205ce7a9bbeb14260dd138a45

Access comprehensive regulatory information for "Nidek" corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e6a5f2205ce7a9bbeb14260dd138a45 and manufactured by NIDEK TECHNOLOGIES S.R.L.. 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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9e6a5f2205ce7a9bbeb14260dd138a45
Registration Details
Taiwan FDA Registration: 9e6a5f2205ce7a9bbeb14260dd138a45
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Device Details

"Nidek" corneal mapper (unsterilized)
TW: โ€œๅฐผๅพทๅ…‹โ€ ่ง’่†œๅœฐๅœ–ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9e6a5f2205ce7a9bbeb14260dd138a45

DHA04400876702

Company Information

Italy

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmology

M.1350 Coratoscope

import

Dates and Status

Apr 23, 2010

Apr 23, 2025

Sep 30, 2021

Cancellation Information

Logged out

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