Taiwan FDA registration 9837be78e526a83e3963b62b63b659be
"Alcon" multi-piece flexible intraocular lens (can filter part of blue light)
TW: “愛爾康”可舒視然多片型軟式人工水晶體(可濾部份藍光)
Taiwan·Risk Class 3·ALCON RESEARCH, LTD.·Registered Aug 27, 2007 – Aug 27, 2022CancelledRegistration details
- Analysis ID
- 9837be78e526a83e3963b62b63b659be
- Customs Code
- DHA00601821603
Company information
- Manufacturer
- ALCON RESEARCH, LTD.
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
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
- import
Dates and status
- Registration Date
- Aug 27, 2007
- Expiry Date
- Aug 27, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Alcon" multi-piece flexible intraocular lens (can filter part of blue light) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9837be78e526a83e3963b62b63b659be and manufactured by ALCON RESEARCH, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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