Taiwan FDA registration e31f07d723f6e331f8437f44ed5bde64

"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 AG·Registered May 27, 2020 – May 27, 2025Expired
Registration details
Analysis ID
e31f07d723f6e331f8437f44ed5bde64
Customs Code
DHA05603360201
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
May 27, 2020
Expiry Date
May 27, 2025
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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 e31f07d723f6e331f8437f44ed5bde64 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. 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 SAS, 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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