Taiwan FDA registration ffc4228d098e0eea39bba19776c973dc
"Zeiss" hydrophobic acrylate posterior chamber intraocular lens
TW: “蔡司”疏水性丙烯酸脂後房人工水晶體
Taiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.·Registered Mar 26, 2020 – Mar 26, 2025ExpiredRegistration details
- Analysis ID
- ffc4228d098e0eea39bba19776c973dc
- Customs Code
- DHA05603333606
Company information
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
Product details
- 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
Dates and status
- Registration Date
- Mar 26, 2020
- Expiry Date
- Mar 26, 2025
About this record
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.
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