Taiwan FDA registration 35beea2426fa9ddee8899bc448ef106b

"Zeiss" Laura Extended Astigmatism Correction of Hydrophilic Posterior Chamber Intraocular Lens

TW: “蔡司”蘿拉景深延長散光矯正親水性後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG·Registered Mar 26, 2021 – Mar 26, 2026Expired
Registration details
Analysis ID
35beea2426fa9ddee8899bc448ef106b
Customs Code
DHA05603447400
Company information
Manufacturer Country
Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
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
Input;; Contract manufacturing
Dates and status
Registration Date
Mar 26, 2021
Expiry Date
Mar 26, 2026
About this record

Access comprehensive regulatory information for "Zeiss" Laura Extended Astigmatism Correction of Hydrophilic 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 35beea2426fa9ddee8899bc448ef106b and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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