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“OPTIKON” Keratron Corneal Topographer (Non-sterile) - Taiwan Registration 9e50c71e53ca64c7306a31bf66b0cc6e

Access comprehensive regulatory information for “OPTIKON” Keratron Corneal Topographer (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 9e50c71e53ca64c7306a31bf66b0cc6e and manufactured by OPTIKON 2000 S. P. A.. The authorized representative in Taiwan is WINSTON MEDICAL SUPPLY CO., LTD..

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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9e50c71e53ca64c7306a31bf66b0cc6e
Registration Details
Taiwan FDA Registration: 9e50c71e53ca64c7306a31bf66b0cc6e
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Device Details

“OPTIKON” Keratron Corneal Topographer (Non-sterile)
TW: “奧帝康”科瑞創角膜地圖儀 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

9e50c71e53ca64c7306a31bf66b0cc6e

Ministry of Health Medical Device Import No. 013820

DHA09401382006

Company Information

Italy

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Jan 28, 2014

Jan 28, 2019

Jan 14, 2019

Cancellation Information

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