Taiwan FDA registration e815c36fea168b8ffb47d8cb062662a6
"Motan" Morgan Eye Surgical Perfusion Device (Unsterilized)
TW: “摩坦”摩根眼科手術灌注裝置 (未滅菌)
Taiwan·Risk Class 1·MORTAN, INC.·Registered Sep 15, 2008 – Sep 15, 2013CancelledRegistration details
- Analysis ID
- e815c36fea168b8ffb47d8cb062662a6
- Customs Code
- DHA04400707000
Company information
- Manufacturer
- MORTAN, INC.
- Manufacturer Country
- United States
- Authorized Representative
- OCARE 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
- Sep 15, 2008
- Expiry Date
- Sep 15, 2013
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Motan" Morgan 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 e815c36fea168b8ffb47d8cb062662a6 and manufactured by MORTAN, INC.. The authorized representative in Taiwan is OCARE LTD..
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