Taiwan FDA registration ab330a4642187fce02a2982981d552b5
"Medica" eye surgical perfusion device (unsterilized)
TW: "美迪卡"眼睛手術灌注裝置(未滅菌)
Taiwan·Risk Class 1·MEDICEL AT·Registered Aug 29, 2011 – Aug 29, 2016CancelledRegistration details
- Analysis ID
- ab330a4642187fce02a2982981d552b5
- Customs Code
- DHA04401076809
Company information
- Manufacturer
- MEDICEL AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Eye Surgical Perfusion Device (M.4360)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4360 Perfusion device for ophthalmic surgery
- Import Information
- import
Dates and status
- Registration Date
- Aug 29, 2011
- Expiry Date
- Aug 29, 2016
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medica" eye surgical perfusion device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab330a4642187fce02a2982981d552b5 and manufactured by MEDICEL AT. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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