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"EyeSys" Corneal Topography (Non-Sterile) - Taiwan Registration 249b759ad0a530f76b21283e2141c602

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 249b759ad0a530f76b21283e2141c602 and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..

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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249b759ad0a530f76b21283e2141c602
Registration Details
Taiwan FDA Registration: 249b759ad0a530f76b21283e2141c602
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Device Details

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

Registration Details

249b759ad0a530f76b21283e2141c602

Ministry of Health Medical Device Import No. 014352

DHA09401435204

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Jul 22, 2014

Jul 22, 2019

Jun 22, 2022

Cancellation Information

Logged out

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