Taiwan FDA registration 764cd0f073eebe0385830970207922b1

"Eye Care" adds visual astigmatism correction monolithic folding intraocular lens

TW: “眼力健”添視明散光矯正單片型折疊式人工水晶體
Taiwan flagTaiwan·Risk Class 3·Johnson & Johnson surgical Vision, Inc.;; AMO Groningen B.V.·Registered Jan 05, 2012 – Jan 05, 2027Active
Registration details
Analysis ID
764cd0f073eebe0385830970207922b1
Customs Code
DHA00602315605
Company information
Manufacturer Country
United States;;Netherlands
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
For ophthalmologist use only (with prescription from an ophthalmologist); input
Dates and status
Registration Date
Jan 05, 2012
Expiry Date
Jan 05, 2027
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About this record

Access comprehensive regulatory information for "Eye Care" adds visual astigmatism correction monolithic folding 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 764cd0f073eebe0385830970207922b1 and manufactured by Johnson & Johnson surgical Vision, Inc.;; AMO Groningen B.V.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Johnson & Johnson surgical Vision, Inc.;; AMO Puerto Rico Manufacturing, Inc., 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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