Taiwan FDA registration ec6e9c117a818b79c9ddfdea182bdd51

"Zeiss" hydrophilic posterior chamber intraocular lens

TW: “蔡司” 親水性後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS·Registered Feb 17, 2023 – Feb 17, 2028Active
Registration details
Analysis ID
ec6e9c117a818b79c9ddfdea182bdd51
Customs Code
DHA05603631003
Company information
Manufacturer Country
France;;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
import
Dates and status
Registration Date
Feb 17, 2023
Expiry Date
Feb 17, 2028
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About this record

Access comprehensive regulatory information for "Zeiss" 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 ec6e9c117a818b79c9ddfdea182bdd51 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG, 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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