"Zeiss" Toby astigmatism corrects hydrophilic posterior chamber intraocular lenses
- Analysis ID
- 3b982c107b502656f6a4d80f4457a3a4
- Customs Code
- DHA05603544508
- Manufacturer
- CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG
- Manufacturer Country
- 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
- Input;; Contract manufacturing
- Registration Date
- Jun 07, 2022
- Expiry Date
- Jun 07, 2027
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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.