Taiwan FDA registration 33e25c6d55e390a83ec5dacd433c7485

"Metroton" Eye Surgical Perfusion Device (Unsterilized)

TW: “美特力敦”眼睛手術灌注裝置 (未滅菌)

Taiwan·Risk Class 1·MEDTRONIC XOMED, INC.·Registered Apr 17, 2009 – Apr 17, 2014Cancelled

Registration details

Analysis ID: 33e25c6d55e390a83ec5dacd433c7485
Customs Code: DHA04400764305

Company information

Manufacturer: MEDTRONIC XOMED, INC.
Manufacturer Country: United States
Authorized Representative: TAIWAN HWA IN ENTERPRISE 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: Apr 17, 2009
Expiry Date: Apr 17, 2014
Cancellation Date: Nov 15, 2016

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Metroton" 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 33e25c6d55e390a83ec5dacd433c7485 and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..

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