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McKovei aortic balloon catheter - Taiwan Registration 12d04009badfd7658698820d97ea628c

Access comprehensive regulatory information for McKovei aortic balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12d04009badfd7658698820d97ea628c and manufactured by DATASCOPE CORP.. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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12d04009badfd7658698820d97ea628c
Registration Details
Taiwan FDA Registration: 12d04009badfd7658698820d97ea628c
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Device Details

McKovei aortic balloon catheter
TW: ้‚ๆŸฏๅ”ฏไธปๅ‹•่„ˆ็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

12d04009badfd7658698820d97ea628c

DHA00602317305

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.3535 Intraarchary Aortic Balloon Dilation and Control System

import

Dates and Status

Dec 22, 2011

Dec 22, 2021

Aug 28, 2023

Cancellation Information

Logged out

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