"McVi" Utima 2nd generation main chest dilator (unsterilized) - Taiwan Registration 76205838b8ee147af930bb930fb07afd
Access comprehensive regulatory information for "McVi" Utima 2nd generation main chest dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76205838b8ee147af930bb930fb07afd and manufactured by MAQUET PUERTO RICO INC.. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.
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
Apr 21, 2006
Apr 21, 2011
Nov 16, 2012
Cancellation Information
Logged out
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