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"Nidek" digital corner mirror - Taiwan Registration 94058e2a4d60232b4784fc7100bc5eb0

Access comprehensive regulatory information for "Nidek" digital corner mirror in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94058e2a4d60232b4784fc7100bc5eb0 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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94058e2a4d60232b4784fc7100bc5eb0
Registration Details
Taiwan FDA Registration: 94058e2a4d60232b4784fc7100bc5eb0
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Device Details

"Nidek" digital corner mirror
TW: โ€œๅฐผๅพทๅ…‹โ€ๆ•ธไฝ้š…่ง’้ก
Risk Class 2

Registration Details

94058e2a4d60232b4784fc7100bc5eb0

DHA05603332106

Company Information

Product Details

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

M Ophthalmology

M.1120 ophthalmic camera;; M.1660 boresight angle prism

import

Dates and Status

Mar 16, 2020

Mar 16, 2030