Taiwan FDA registration e8b74a32e42c5db6a777055dc3cbef83
"Alcon" flexible intraocular lens implantation system
TW: "愛爾康"可舒軟式人工水晶體植入系統
Taiwan·Risk Class 1·ALCON MANUFACTURING, LTD.·Registered Oct 30, 2005 – Oct 30, 2010CancelledRegistration details
- Analysis ID
- e8b74a32e42c5db6a777055dc3cbef83
- Customs Code
- DHA04400143201
Company information
- Manufacturer
- ALCON MANUFACTURING, LTD.
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- An intraocular lens guide is a device that is placed into the eye to guide intraocular lens insertion during surgery and can be removed when surgery is completed.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Oct 30, 2005
- Expiry Date
- Oct 30, 2010
- Cancellation Date
- Nov 19, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Alcon" flexible intraocular lens implantation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8b74a32e42c5db6a777055dc3cbef83 and manufactured by ALCON MANUFACTURING, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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