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"McKovei" aortic balloon catheter - Taiwan Registration 4fda4b2aad1e319bee4243ef621f9fef

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 3 medical device is registered under number 4fda4b2aad1e319bee4243ef621f9fef 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, 1 companies making similar products including DATASCOPE CORP., 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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4fda4b2aad1e319bee4243ef621f9fef
Registration Details
Taiwan FDA Registration: 4fda4b2aad1e319bee4243ef621f9fef
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Device Details

"McKovei" aortic balloon catheter
TW: "้‚ๆŸฏๅ”ฏ"ไธปๅ‹•่„ˆๆฐฃ็ƒๅฐŽ็ฎก
Risk Class 3

Registration Details

4fda4b2aad1e319bee4243ef621f9fef

DHA00601024904

Company Information

United States

Product Details

E Cardiovascular Medicine Science

import

Dates and Status

Mar 21, 2003

Mar 21, 2028

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