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Software - ANVISA Registration 80071260410

Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80071260410 and manufactured by GE HEALTHCARE FINLAND OY. 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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80071260410
Registration Details
ANVISA Registration Number: 80071260410
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Device Details

Centricity High Acuity Anesthesia
Risk Class II

Registration Details

80071260410

25351521424201972

00029372000140

Company Information

Finland
PT: FINLร‚NDIA

Dates and Status

Jan 30, 2020

VIGENTE

09/18/2025 19:00:01