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"Nidek" Digital PD Meter(Non-Sterile) - Taiwan Registration e533781ddf091a4a09876d941ee68ad8

Access comprehensive regulatory information for "Nidek" Digital PD Meter(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e533781ddf091a4a09876d941ee68ad8 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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e533781ddf091a4a09876d941ee68ad8
Registration Details
Taiwan FDA Registration: e533781ddf091a4a09876d941ee68ad8
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Device Details

"Nidek" Digital PD Meter(Non-Sterile)
TW: "ๅฐผๅพทๅ…‹"็žณ่ทๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e533781ddf091a4a09876d941ee68ad8

Ministry of Health Medical Device Import Registration No. 010246

DHA08401024602

Company Information

Japan

Product Details

Limited to the first level recognition range of the "Pupil Meter (M.1700)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1700 Pupillometer

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026