"Zeiss" hydrophobic acrylate posterior chamber intraocular lens - Taiwan Registration ffc4228d098e0eea39bba19776c973dc
Access comprehensive regulatory information for "Zeiss" hydrophobic acrylate 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 ffc4228d098e0eea39bba19776c973dc and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
This page provides complete technical specifications, regulatory compliance details. 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
ffc4228d098e0eea39bba19776c973dc
Registration Details
Taiwan FDA Registration: ffc4228d098e0eea39bba19776c973dc
Device Details
"Zeiss" hydrophobic acrylate posterior chamber intraocular lens
TW: โ่กๅธโ็ๆฐดๆงไธ็ฏ้
ธ่ๅพๆฟไบบๅทฅๆฐดๆถ้ซ
Risk Class 3

