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"Medtronic" Enray aortic stent system - Taiwan Registration 659700e704ebfe187b70db6c3dc88436

Access comprehensive regulatory information for "Medtronic" Enray 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 659700e704ebfe187b70db6c3dc88436 and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC VASCULAR, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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659700e704ebfe187b70db6c3dc88436
Registration Details
Taiwan FDA Registration: 659700e704ebfe187b70db6c3dc88436
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Device Details

"Medtronic" Enray aortic stent system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅฎ‰็‘žไธปๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

659700e704ebfe187b70db6c3dc88436

DHA00601896100

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Mar 04, 2008

Mar 04, 2013

Nov 15, 2016

Cancellation Information

Logged out

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