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"Nidek" multi-wavelength fundus photocoagulation laser - Taiwan Registration 90d40a49fd9863c77ee5aad68bd7519e

Access comprehensive regulatory information for "Nidek" multi-wavelength fundus photocoagulation laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90d40a49fd9863c77ee5aad68bd7519e 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.

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90d40a49fd9863c77ee5aad68bd7519e
Registration Details
Taiwan FDA Registration: 90d40a49fd9863c77ee5aad68bd7519e
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Device Details

"Nidek" multi-wavelength fundus photocoagulation laser
TW: โ€œๅฐผๅพทๅ…‹โ€ๅคšๆณข้•ท็œผๅบ•ๅ…‰ๅ‡้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

90d40a49fd9863c77ee5aad68bd7519e

DHA00602063502

Company Information

Product Details

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

M Ophthalmology

M.4690 ็œผ็ง‘็”จๅ…‰ๅ‡ๅ›บๅ„€

import

Dates and Status

Mar 08, 2010

Mar 08, 2015

Apr 13, 2018

Cancellation Information

Logged out

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