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Magnetic Resonance Imaging Equipment - ANVISA Registration 80005260011

Access comprehensive regulatory information for Magnetic Resonance Imaging Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80005260011 and manufactured by FUJIFILM HEALTHCARE CORPORATION. The registration is held by FUJIFILM HEALTHCARE DO BRASIL 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 SIEMENS HEALTHCARE GMBH, GE MEDICAL SYSTEMS LLC, 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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80005260011
Registration Details
ANVISA Registration Number: 80005260011
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Device Details

SISTEMA DE IMAGEM POR RESSONÂNCIA MAGNÉTICA
Risk Class II

Registration Details

80005260011

25351150765201347

02517363000124

Company Information

Japan
PT: JAPÃO

Dates and Status

Aug 26, 2013

VIGENTE

09/18/2025 19:00:01