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"EyeSys" Corneal Topography (Non-Sterile) - Taiwan Registration e81e4824d7998a52999132f273d07aa6

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 e81e4824d7998a52999132f273d07aa6 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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e81e4824d7998a52999132f273d07aa6
Registration Details
Taiwan FDA Registration: e81e4824d7998a52999132f273d07aa6
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Device Details

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

Registration Details

e81e4824d7998a52999132f273d07aa6

Ministry of Health Medical Device Import Registration No. 018982

DHA08401898209

Company Information

United States

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023

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