"Kedir" cardiovascular surgical instrument (unsterilized) - Taiwan Registration 55bed855431600b4dc7f8a68130836ee
Access comprehensive regulatory information for "Kedir" cardiovascular surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55bed855431600b4dc7f8a68130836ee and manufactured by CARDIOMEDICAL GMBH. The authorized representative in Taiwan is ANSON HEALTH CARE INC..
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.
Device Details
Product Details
It is limited to the scope of first-class identification of cardiovascular surgical devices (E.4500) in the Measures for the Administration of Medical Devices.
E Cardiovascular Medicine Science
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import
Dates and Status
May 10, 2006
May 10, 2011
Dec 03, 2012
Cancellation Information
Logged out
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