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"Arno" intra-aortic balloon pump - Taiwan Registration 0109ade5a956c9e23a8810075b3727de

Access comprehensive regulatory information for "Arno" intra-aortic balloon pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0109ade5a956c9e23a8810075b3727de and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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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0109ade5a956c9e23a8810075b3727de
Registration Details
Taiwan FDA Registration: 0109ade5a956c9e23a8810075b3727de
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Device Details

"Arno" intra-aortic balloon pump
TW: โ€œไบž่ซพโ€ไธปๅ‹•่„ˆๅ…งๆฐฃ็ƒๅนซๆตฆ
Risk Class 3

Registration Details

0109ade5a956c9e23a8810075b3727de

DHA00602161004

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

Oct 29, 2010

Oct 29, 2025