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“TAKAGI” Contrast Glaretester (Non-Sterile) - Taiwan Registration 314a23151007c59b2e2c3e5ef831c0f2

Access comprehensive regulatory information for “TAKAGI” Contrast Glaretester (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 314a23151007c59b2e2c3e5ef831c0f2 and manufactured by TAKAGI SEIKO 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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314a23151007c59b2e2c3e5ef831c0f2
Registration Details
Taiwan FDA Registration: 314a23151007c59b2e2c3e5ef831c0f2
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Device Details

“TAKAGI” Contrast Glaretester (Non-Sterile)
TW: “高木精工”對比眩光測試儀 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

314a23151007c59b2e2c3e5ef831c0f2

Ministry of Health Medical Device Import No. 014554

DHA09401455403

Company Information

Japan

Product Details

M Ophthalmic devices

M1460 stereo sensor

Imported from abroad

Dates and Status

Oct 08, 2014

Oct 08, 2024

Cancellation Information

Logged out

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