Taiwan FDA registration 911c38245519a35ee6cd8a72e1684203

"Alcon Ireland Factory" can comfort monolithic flexible intraocular lens

TW: “愛爾康愛爾蘭廠”可舒單片型軟式人工水晶體
Taiwan flagTaiwan·Risk Class 3·ALCON LABORATORIES IRELAND LIMITED·Registered Nov 26, 2010 – Nov 26, 2025Expired
Registration details
Analysis ID
911c38245519a35ee6cd8a72e1684203
Customs Code
DHA00602174909
Company information
Manufacturer Country
Ireland
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
Nov 26, 2010
Expiry Date
Nov 26, 2025
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About this record

Access comprehensive regulatory information for "Alcon Ireland Factory" can comfort monolithic flexible intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 911c38245519a35ee6cd8a72e1684203 and manufactured by ALCON LABORATORIES IRELAND LIMITED. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ALCON LABORATORIES IRELAND LIMITED, and 1 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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