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Ultrasound Device - ANVISA Registration 80071260351

Access comprehensive regulatory information for Ultrasound Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80071260351 and manufactured by GE ULTRASOUND KOREA, LTD. 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 VINNO TECHNOLOGY (SUZHOU) CO. LTD., SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS 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.

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80071260351
Registration Details
ANVISA Registration Number: 80071260351
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Device Details

Sistema de Ultrassom Logiq
Risk Class II

Registration Details

80071260351

25351288357201522

00029372000140

Company Information

South Korea
PT: CORร‰IA DO SUL

Dates and Status

Jul 13, 2015

VIGENTE

09/18/2025 19:00:01