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“TAKAGI”Perimeter( Non-Sterile) - Taiwan Registration 202cb1305b09cc9ed5fb1648e7656504

Access comprehensive regulatory information for “TAKAGI”Perimeter( 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 202cb1305b09cc9ed5fb1648e7656504 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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202cb1305b09cc9ed5fb1648e7656504
Registration Details
Taiwan FDA Registration: 202cb1305b09cc9ed5fb1648e7656504
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Device Details

“TAKAGI”Perimeter( Non-Sterile)
TW: “高木精工”視野計(未滅菌)
Risk Class 1
MD

Registration Details

202cb1305b09cc9ed5fb1648e7656504

Ministry of Health Medical Device Import Registration No. 008876

DHA08400887604

Company Information

Japan

Product Details

Limited to the first-level identification range of the "Visual Field Scope (M.1605)" of the Measures for the Administration of Medical Equipment.

M Ophthalmic devices

M1605 field of view mirror

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025