Guide Wire - ANVISA Registration 10324860023

Access comprehensive regulatory information for 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 10324860023 and manufactured by NIPRO MEDICAL INDUSTRIES LTDA. The registration is held by NIPRO MEDICAL LTDA with validity until Apr 30, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SP MEDICAL A/S, and 5 recent registrations in the same technical category. 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.