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"Nidek" diode laser solidifier - Taiwan Registration 8dfa963418c020382ac08b55f8eecf8f

Access comprehensive regulatory information for "Nidek" diode laser solidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8dfa963418c020382ac08b55f8eecf8f 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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8dfa963418c020382ac08b55f8eecf8f
Registration Details
Taiwan FDA Registration: 8dfa963418c020382ac08b55f8eecf8f
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Device Details

"Nidek" diode laser solidifier
TW: "ๅฐผๅพทๅ…‹"ไบŒๆฅต้ซ”้›ทๅฐ„ๅ…‰ๅ‡ๅ›บๅ„€
Risk Class 2
Cancelled

Registration Details

8dfa963418c020382ac08b55f8eecf8f

DHA00601433201

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

import

Dates and Status

Apr 21, 2006

Apr 21, 2016

Apr 13, 2018

Cancellation Information

Logged out

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