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"EyeSys" Corneal Topography (Non-Sterile) - Taiwan Registration 84c43b8ce967c0a7431caae9e7b5bab8

Access comprehensive regulatory information for "EyeSys" Corneal Topography (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 84c43b8ce967c0a7431caae9e7b5bab8 and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EYESYS VISION, INC., and 2 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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84c43b8ce967c0a7431caae9e7b5bab8
Registration Details
Taiwan FDA Registration: 84c43b8ce967c0a7431caae9e7b5bab8
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Device Details

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

Registration Details

84c43b8ce967c0a7431caae9e7b5bab8

Ministry of Health Medical Device Import No. 018982

DHA09401898205

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Apr 18, 2018

Apr 18, 2023

Cancellation Information

Logged out

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