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"TAKAGI" View Tester(Non-Sterile) - Taiwan Registration 589e96af77b644c6ce0ff649aeaf79f9

Access comprehensive regulatory information for "TAKAGI" View Tester(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 589e96af77b644c6ce0ff649aeaf79f9 and manufactured by TAKAGI SEIKO CO., LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL 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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589e96af77b644c6ce0ff649aeaf79f9
Registration Details
Taiwan FDA Registration: 589e96af77b644c6ce0ff649aeaf79f9
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Device Details

"TAKAGI" View Tester(Non-Sterile)
TW: "้ซ˜ๆœจ"่‡ช่ฆบๅผ้ฉ—ๅ…‰ๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

589e96af77b644c6ce0ff649aeaf79f9

Ministry of Health Medical Device Import Registration No. 002941

DHA08400294101

Company Information

Japan

Product Details

A manual refractometer is a group of lenses of different refractive intensities to measure refractive errors in the eye.

M Ophthalmic devices

M1770 Manual Fold Meter

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026