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"CANON" FULL AUTO REF-KERATOMETER (Non-Sterile) - Taiwan Registration e66f99d5687bafff3972ae4484c3d638

Access comprehensive regulatory information for "CANON" FULL AUTO REF-KERATOMETER (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 e66f99d5687bafff3972ae4484c3d638 and manufactured by CANON COMPONENTS,INC.. The authorized representative in Taiwan is CLINICO INC..

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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e66f99d5687bafff3972ae4484c3d638
Registration Details
Taiwan FDA Registration: e66f99d5687bafff3972ae4484c3d638
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Device Details

"CANON" FULL AUTO REF-KERATOMETER (Non-Sterile)
TW: "ไฝณ่ƒฝ" ๅ…จ่‡ชๅ‹•้›ป่…ฆ้ฉ—ๅ…‰ๅŠ่ง’่†œๅผงๅบฆๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e66f99d5687bafff3972ae4484c3d638

Ministry of Health Medical Device Import Registration No. 000007

DHA08400000704

Company Information

Japan

Product Details

Measure eye refraction and corneal curvature.

M Ophthalmic devices

M1760 Ophthalmic Refractive Machine

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025