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"Medtronic" Van Ren Dena Vion thoracic aortic stent system - Taiwan Registration b0c8fe7887a37d4b6ee119eb19ac6271

Access comprehensive regulatory information for "Medtronic" Van Ren Dena Vion thoracic aortic stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b0c8fe7887a37d4b6ee119eb19ac6271 and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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b0c8fe7887a37d4b6ee119eb19ac6271
Registration Details
Taiwan FDA Registration: b0c8fe7887a37d4b6ee119eb19ac6271
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Device Details

"Medtronic" Van Ren Dena Vion thoracic aortic stent system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€่Œƒๅ€ซ็‰น็ดๅจๆ˜‚่ƒธไธปๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

b0c8fe7887a37d4b6ee119eb19ac6271

DHA05603308609

Company Information

Ireland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0006.

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Jan 07, 2020

Jan 07, 2025