Taiwan FDA registration 3b640a20c9a68ace3497752233f98940

"ZEISS" Lucian aspheric hydrophobic posterior chamber intraocular lens

TW: “蔡司” 露西亞非球面疏水性後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.·Registered Feb 05, 2024 – Feb 05, 2029Active
Registration details
Analysis ID
3b640a20c9a68ace3497752233f98940
Customs Code
DHA05603691804
Company information
Manufacturer Country
United States;;Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.3600 Artificial Crystal
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Feb 05, 2024
Expiry Date
Feb 05, 2029
About this record

Access comprehensive regulatory information for "ZEISS" Lucian aspheric hydrophobic posterior chamber 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 3b640a20c9a68ace3497752233f98940 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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