Pure Global

Electrocardiograph - ANVISA Registration 80303619001

Access comprehensive regulatory information for Electrocardiograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80303619001 and manufactured by CARDIOLINE SPA. The registration is held by AURION EQUIPAMENTOS ELETRÔNICOS LTDA -ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including CONTEC MEDICAL SYSTEMS CO., LTD., BIONET (SHINSEGAE) CO., LTD, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80303619001
Registration Details
ANVISA Registration Number: 80303619001
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Eletrocardiógrafo
Risk Class II

Registration Details

80303619001

25351793813201657

06889652000105

Company Information

CARDIOLINE SPA
Italy
PT: ITÁLIA

Dates and Status

May 02, 2016

VIGENTE

09/18/2025 19:00:01