Taiwan FDA registration d95db9c0ad684ce0088c875448e20448
"Meidus" IOL guide (sterilization)
TW: "美德思" 人工水晶體導引器(滅菌)
Taiwan·Risk Class 1·ROBUTEC AG;; MEDICEL AG·Registered Jan 18, 2023 – Jan 18, 2028ActiveRegistration details
- Analysis ID
- d95db9c0ad684ce0088c875448e20448
- Customs Code
- DHA09402301908
Company information
- Manufacturer
- ROBUTEC AG;; MEDICEL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- CONEYE 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
- Jan 18, 2023
- Expiry Date
- Jan 18, 2028
About this record
Access comprehensive regulatory information for "Meidus" IOL 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 d95db9c0ad684ce0088c875448e20448 and manufactured by ROBUTEC AG;; MEDICEL AG. The authorized representative in Taiwan is CONEYE CO., LTD.
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