Taiwan FDA registration a23075a6eea360e4a9e66272f103e469
"Fasio" intraocular lens guide (sterilization)
TW: "法西歐" 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·PHYSIOL S.A.·Registered Nov 25, 2016 – Nov 25, 2026ActiveRegistration details
- Analysis ID
- a23075a6eea360e4a9e66272f103e469
- Customs Code
- DHA09401720901
Company information
- Manufacturer
- PHYSIOL S.A.
- Manufacturer Country
- Belgium
- Authorized Representative
- CHIU HO SCIENTIFIC CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 25, 2016
- Expiry Date
- Nov 25, 2026
About this record
Access comprehensive regulatory information for "Fasio" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a23075a6eea360e4a9e66272f103e469 and manufactured by PHYSIOL S.A.. The authorized representative in Taiwan is CHIU HO SCIENTIFIC CO., LTD..
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