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"Alcon" can be sutoremine astigmatism correction monolithic flexible intraocular lens (can filter part of blue light) - Taiwan Registration e9b7b6822db21ce914503c08712308db

Access comprehensive regulatory information for "Alcon" can be sutoremine astigmatism correction monolithic flexible intraocular lens (can filter part of blue light) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e9b7b6822db21ce914503c08712308db and manufactured by ALCON RESEARCH, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

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e9b7b6822db21ce914503c08712308db
Registration Details
Taiwan FDA Registration: e9b7b6822db21ce914503c08712308db
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Device Details

"Alcon" can be sutoremine astigmatism correction monolithic flexible intraocular lens (can filter part of blue light)
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Risk Class 3
Cancelled

Registration Details

e9b7b6822db21ce914503c08712308db

DHA00601826901

Company Information

United States

Product Details

It is mainly suitable for the first implantation of intraocular crystal sac to correct the vision of existing corneal astigmatism and amorphous patients, and can also be applied to adult patients regardless of presbyopia, after cataract removal, want to promote uncorrected distance vision and reduce residual columnar refraction, and reduce dependence on glasses during distance vision.

M Ophthalmology

M.3600 Artificial Crystal

import

Dates and Status

May 25, 2007

May 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

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