Taiwan FDA registration 333a1094182fb50b0b4ecf3ef045f164
"Fasio" IOL guide (unsterilized)
TW: "法西歐" 人工水晶體導引器 (未滅菌)
Taiwan·Risk Class 1·PhysIOL s.a.·Registered Oct 04, 2016 – Oct 04, 2021CancelledRegistration details
- Analysis ID
- 333a1094182fb50b0b4ecf3ef045f164
- Customs Code
- DHA09401705105
Company information
- Manufacturer
- PhysIOL s.a.
- Manufacturer Country
- Belgium
- Authorized Representative
- CHIU HO MEDICAL SYSTEM CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2016
- Expiry Date
- Oct 04, 2021
- Cancellation Date
- Jan 11, 2023
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延;;自請註銷
About this record
Access comprehensive regulatory information for "Fasio" IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 333a1094182fb50b0b4ecf3ef045f164 and manufactured by PhysIOL s.a.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..
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