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“Alcon” LenSx Laser Patient Interface - Taiwan Registration ee5cd2eaaec051cc8d83a989e180c1b2

Access comprehensive regulatory information for “Alcon” LenSx Laser Patient Interface in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee5cd2eaaec051cc8d83a989e180c1b2 and manufactured by Alcon Research, LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

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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ee5cd2eaaec051cc8d83a989e180c1b2
Registration Details
Taiwan FDA Registration: ee5cd2eaaec051cc8d83a989e180c1b2
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Device Details

“Alcon” LenSx Laser Patient Interface
TW: “愛爾康” 雷視能雷射患者介面
Risk Class 2
MD

Registration Details

ee5cd2eaaec051cc8d83a989e180c1b2

Ministry of Health Medical Device Import No. 030784

DHA05603078405

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M4390 Ophthalmic laser unit

Imported from abroad

Dates and Status

Mar 27, 2018

Mar 27, 2028