Taiwan FDA registration c1489095049cd23bc73fc152f0df0f46
"Medis" intraocular lens guide (sterilization)
TW: "麥迪斯" 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·MEDICEL AT·Registered Feb 18, 2013 – Feb 18, 2018CancelledRegistration details
- Analysis ID
- c1489095049cd23bc73fc152f0df0f46
- Customs Code
- DHA04401270801
Company information
- Manufacturer
- MEDICEL AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 18, 2013
- Expiry Date
- Feb 18, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medis" 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 c1489095049cd23bc73fc152f0df0f46 and manufactured by MEDICEL AT. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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