Taiwan FDA registration eb862b9ec26e63ca5f26cdddcc92437d
"ZEISS" Alana trifocal hydrophobic posterior chamber intraocular lens
TW: “蔡司” 艾拉娜三焦點疏水性後房人工水晶體
Taiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG·Registered Feb 02, 2024 – Feb 02, 2029ActiveRegistration details
- Analysis ID
- eb862b9ec26e63ca5f26cdddcc92437d
- Customs Code
- DHA05603691702
Company information
- Manufacturer
- CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG
- Manufacturer Country
- Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
Product details
- 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
Dates and status
- Registration Date
- Feb 02, 2024
- Expiry Date
- Feb 02, 2029
About this record
Access comprehensive regulatory information for "ZEISS" Alana trifocal 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 eb862b9ec26e63ca5f26cdddcc92437d and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
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