Patient Monitoring System - ANVISA Registration 80224390258

Access comprehensive regulatory information for Patient Monitoring System in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80224390258 and manufactured by BIOTRONIK SE & CO KG. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Sep 12, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MGC DIAGNOSTICS CORPORATION, HILL-ROM CLINICAL WORKFLOW SOLUTIONS, 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.