Taiwan FDA registration d12fed16cc4fc9876341766a068cce6f
Neo-Siss focal intraocular lenses
TW: 新西斯延焦人工水晶體
Registration details
- Analysis ID
- d12fed16cc4fc9876341766a068cce6f
- Customs Code
- DHA05603577901
Company information
- Manufacturer Country
- France
- Authorized Representative
- CRYSTALVISION CO., LTD.
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
- import
Dates and status
- Registration Date
- Sep 01, 2022
- Expiry Date
- Sep 01, 2027
About this record
Access comprehensive regulatory information for Neo-Siss focal intraocular lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d12fed16cc4fc9876341766a068cce6f and manufactured by Cutting Edge Manufacturing SAS;; Cutting Edge SAS. The authorized representative in Taiwan is CRYSTALVISION CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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