"Zeiss" hydrophilic posterior chamber intraocular lens
- Analysis ID
- e31f07d723f6e331f8437f44ed5bde64
- Customs Code
- DHA05603360201
- Manufacturer
- CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG
- Manufacturer Country
- Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- Input;; Contract manufacturing
- Registration Date
- May 27, 2020
- Expiry Date
- May 27, 2025
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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 e31f07d723f6e331f8437f44ed5bde64 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, 1 companies making similar products including CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec SAS, 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.