Taiwan FDA registration 3b982c107b502656f6a4d80f4457a3a4

"Zeiss" Toby astigmatism corrects hydrophilic posterior chamber intraocular lenses

TW: “蔡司” 托比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 Jun 07, 2022 – Jun 07, 2027Active
Registration details
Analysis ID
3b982c107b502656f6a4d80f4457a3a4
Customs Code
DHA05603544508
Company information
Manufacturer Country
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
Input;; Contract manufacturing
Dates and status
Registration Date
Jun 07, 2022
Expiry Date
Jun 07, 2027
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About this record

Access comprehensive regulatory information for "Zeiss" Toby astigmatism corrects hydrophilic posterior chamber intraocular lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3b982c107b502656f6a4d80f4457a3a4 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, 2 companies making similar products including CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS, CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG, and 2 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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