"Zeiss" Toby astigmatism corrects hydrophilic posterior chamber intraocular lenses - Taiwan Registration 3b982c107b502656f6a4d80f4457a3a4

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.