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"Medtronic" Enray aortic stent system - Taiwan Registration 55a4056d01e76e0bde94bb1e80499375

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 2 medical device is registered under number 55a4056d01e76e0bde94bb1e80499375 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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55a4056d01e76e0bde94bb1e80499375
Registration Details
Taiwan FDA Registration: 55a4056d01e76e0bde94bb1e80499375
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Device Details

"Medtronic" Enray aortic stent system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅฎ‰็‘žไธปๅ‹•่„ˆๆ”ฏๆžถ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

55a4056d01e76e0bde94bb1e80499375

DHA00602044102

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Nov 26, 2009

Nov 26, 2014

Apr 25, 2018

Cancellation Information

Logged out

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