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“NIDEK” Slit Lamp - Taiwan Registration 66686fb91206c0c3dc9cebbcaced0504

Access comprehensive regulatory information for “NIDEK” Slit Lamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66686fb91206c0c3dc9cebbcaced0504 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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66686fb91206c0c3dc9cebbcaced0504
Registration Details
Taiwan FDA Registration: 66686fb91206c0c3dc9cebbcaced0504
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Device Details

“NIDEK” Slit Lamp
TW: “尼德克”裂隙燈
Risk Class 2
MD

Registration Details

66686fb91206c0c3dc9cebbcaced0504

Ministry of Health Medical Device Import No. 030006

DHA05603000609

Company Information

Product Details

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

M Ophthalmic devices

M1850 AC power type fine gap lamp

Imported from abroad

Dates and Status

Aug 10, 2017

Aug 10, 2027