"Alcon" can be sutoremine astigmatism correction monolithic flexible intraocular lens (can filter part of blue light)
Taiwan·Risk Class 3·ALCON RESEARCH, LTD.·Registered May 25, 2007 – May 25, 2022Cancelled- Analysis ID
- e9b7b6822db21ce914503c08712308db
- Customs Code
- DHA00601826901
- Manufacturer
- ALCON RESEARCH, LTD.
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
- Intended Use
- It is mainly suitable for the first implantation of intraocular crystal sac to correct the vision of existing corneal astigmatism and amorphous patients, and can also be applied to adult patients regardless of presbyopia, after cataract removal, want to promote uncorrected distance vision and reduce residual columnar refraction, and reduce dependence on glasses during distance vision.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- import
- Registration Date
- May 25, 2007
- Expiry Date
- May 25, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
Access comprehensive regulatory information for "Alcon" can be sutoremine astigmatism correction monolithic 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 e9b7b6822db21ce914503c08712308db and manufactured by ALCON RESEARCH, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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