Taiwan FDA registration 427feb8a3b532efd379e82cb14e78a2c
"Medix" Microjet intraocular lens guide (unsterilized)
TW: “麥迪斯”微可捷人工水晶體導引器 (未滅菌)
Taiwan·Risk Class 1·MEDICEL AT·Registered Feb 17, 2009 – Feb 17, 2014CancelledRegistration details
- Analysis ID
- 427feb8a3b532efd379e82cb14e78a2c
- Customs Code
- DHA04400749605
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
- import
Dates and status
- Registration Date
- Feb 17, 2009
- Expiry Date
- Feb 17, 2014
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medix" Microjet intraocular lens 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 427feb8a3b532efd379e82cb14e78a2c and manufactured by MEDICEL AT. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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