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Intra-arterial balloon compression system - Taiwan Registration 0725c718af659bcaf6556d6590add72a

Access comprehensive regulatory information for Intra-arterial balloon compression system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0725c718af659bcaf6556d6590add72a and manufactured by KONTRON CARDIOVASCULAR INC.. The authorized representative in Taiwan is ROCHE PRODUCTS LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KONTRON INSTRUMENT, INC., and 2 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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0725c718af659bcaf6556d6590add72a
Registration Details
Taiwan FDA Registration: 0725c718af659bcaf6556d6590add72a
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Device Details

Intra-arterial balloon compression system
TW: ๅ‹•่„ˆๅ…งๆฑฝ็ƒๅฃ“็ธฎ็ณป็ตฑ
Cancelled

Registration Details

0725c718af659bcaf6556d6590add72a

DHA00600553001

Company Information

United States

Product Details

0646 Aortic arch balloon device

import

Dates and Status

Feb 23, 1989

Feb 23, 1994

Oct 03, 1994

Cancellation Information

Logged out

ๆœ‰ๆ•ˆๆœŸ้–“ๅทฒๅฑ†ๆœช่ƒฝ่ฃœไปถ

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