Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Magnetic resonance imaging equipment (MRI) - ANVISA Registration 80071269009

Access comprehensive regulatory information for Magnetic resonance imaging equipment (MRI) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80071269009 and manufactured by GE HEALTHCARE (TIANJIN) COMPANY LIMITED. 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 SIEMENS SHENZHEN MAGNETIC RESONANCE LTD, SIEMENS HEALTHCARE DIAGNOSTICOS 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80071269009
Registration Details
ANVISA Registration Number: 80071269009
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

80071269009

25351683322202164

00029372000140

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 08, 2021

VIGENTE

09/18/2025 19:00:01