"Zeiss" Toby astigmatism corrects hydrophilic posterior chamber intraocular lenses - Taiwan Registration b8a974a8596acccec948556b5aaa180b

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.