Taiwan FDA registration b8a974a8596acccec948556b5aaa180b

"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 15, 2020 – Jun 15, 2025Expired
Registration details
Analysis ID
b8a974a8596acccec948556b5aaa180b
Customs Code
DHA05603376503
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
Contract manufacturing;; input
Dates and status
Registration Date
Jun 15, 2020
Expiry Date
Jun 15, 2025
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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 b8a974a8596acccec948556b5aaa180b 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 AG, CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS, 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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