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"EyeSys" Corneal Topography System (Non-Sterile) - Taiwan Registration a3ef4a5621fd74419cea5c40c6f6baee

Access comprehensive regulatory information for "EyeSys" Corneal Topography System (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 a3ef4a5621fd74419cea5c40c6f6baee and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EYESYS VISION, INC., and 1 recent registrations in the same category. 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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a3ef4a5621fd74419cea5c40c6f6baee
Registration Details
Taiwan FDA Registration: a3ef4a5621fd74419cea5c40c6f6baee
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Device Details

"EyeSys" Corneal Topography System (Non-Sterile)
TW: "ๆ„›่ฆ–" ่ง’่†œๅœฐๅœ–ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a3ef4a5621fd74419cea5c40c6f6baee

Ministry of Health Medical Device Import No. 016285

DHA09401628502

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Mar 22, 2016

Mar 22, 2026

Cancellation Information

Logged out

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