Taiwan FDA registration 26edcaec519ecc6d69d16c850fcc204c

"Zeiss" esfinafil spherical hydrophilic posterior chamber intraocular lens

TW: “蔡司”艾斯菲那非球面親水性後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG·Registered Sep 09, 2020 – Sep 09, 2025Expired
Registration details
Analysis ID
26edcaec519ecc6d69d16c850fcc204c
Customs Code
DHA05603394505
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
Sep 09, 2020
Expiry Date
Sep 09, 2025
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About this record

Access comprehensive regulatory information for "Zeiss" esfinafil spherical 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 26edcaec519ecc6d69d16c850fcc204c 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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