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"INSZO" aortic balloon catheter - Taiwan Registration 5a9657d82d5b83d3c3a9b318163b5c89

Access comprehensive regulatory information for "INSZO" 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 5a9657d82d5b83d3c3a9b318163b5c89 and manufactured by Insightra Medical, Inc.. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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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5a9657d82d5b83d3c3a9b318163b5c89
Registration Details
Taiwan FDA Registration: 5a9657d82d5b83d3c3a9b318163b5c89
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Device Details

"INSZO" aortic balloon catheter
TW: โ€œ่‹ฑๆ–ฏๅ“โ€ไธปๅ‹•่„ˆๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

5a9657d82d5b83d3c3a9b318163b5c89

DHA05602942809

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

Contract manufacturing;; input

Dates and Status

Mar 28, 2017

Mar 28, 2022

Apr 12, 2024

Cancellation Information

Logged out

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