CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 81667100053

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81667100053 and manufactured by SHANGHAI MICROPORT CARDIOFLOW MEDTECHCO., LTD. The registration is held by MICROPORT SCIENTIFIC VASCULAR BRASIL LTDA with validity until Sep 05, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.