Ultrasound diagnostic/imaging equipment - ANVISA Registration 80022060093

Access comprehensive regulatory information for Ultrasound diagnostic/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 80022060093 and manufactured by SONOSITE INC. The registration is held by FUJIFILM DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SIEMENS MEDICAL SOLUTIONS USA, INC., GE MEDICAL SYSTEMS (CHINA) 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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80022060093
Registration Details
ANVISA Registration Number: 80022060093
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

EQUIPAMENTO DE ULTRASSOM SONOSITE EDGE II
Risk Class II

Registration Details

80022060093

25351626945201834

60397874000156

Company Information

SONOSITE INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 24, 2018

VIGENTE

09/18/2025 19:00:01