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Software - ANVISA Registration 80071260397

Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80071260397 and manufactured by GE HEALTHCARE. The registration is held by GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA 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 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., CARDIO SISTEMAS COMERCIAL E INDUSTRIAL LTDA, 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.

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80071260397
Registration Details
ANVISA Registration Number: 80071260397
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Device Details

Centricity Cardio Workflow
Risk Class I

Registration Details

80071260397

25351052126201929

00029372000140

Company Information

GE HEALTHCARE
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

May 08, 2019

VIGENTE

09/18/2025 19:00:01