"ZEISS" Lucian aspheric hydrophobic posterior chamber intraocular lens
- Analysis ID
- 3b640a20c9a68ace3497752233f98940
- Customs Code
- DHA05603691804
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
- 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
- Contract manufacturing;; input
- Registration Date
- Feb 05, 2024
- Expiry Date
- Feb 05, 2029
Access comprehensive regulatory information for "ZEISS" Lucian aspheric hydrophobic 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 3b640a20c9a68ace3497752233f98940 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.