"Zeiss" hydrophilic posterior chamber intraocular lens
- Analysis ID
- ec6e9c117a818b79c9ddfdea182bdd51
- Customs Code
- DHA05603631003
- Manufacturer
- CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS
- Manufacturer Country
- France;;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
- import
- Registration Date
- Feb 17, 2023
- Expiry Date
- Feb 17, 2028
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Access comprehensive regulatory information for "Zeiss" hydrophilic 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 ec6e9c117a818b79c9ddfdea182bdd51 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG, and 1 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.