Software - ANVISA Registration 80042070040
Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80042070040 and manufactured by BRAINLAB AG. The registration is held by BRAINLAB 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 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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Registration Details
80042070040
25351531037201552
02981566000177
Company Information
Dates and Status
Oct 26, 2015
VIGENTE
09/18/2025 19:00:01
Software
patient on line
FRESENIUS MEDICAL CARE AG
80133950142
May 09, 2019
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81504790259
May 20, 2021
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81464750166
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81901710005
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EDAN INSTRUMENTS, INC
80047300752
Mar 19, 2020
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.• Netherlands
CARDIO SISTEMAS COMERCIAL E INDUSTRIAL LTDA• Brazil
GE HEALTHCARE IITS USA CORP• United States of America
AGFA HEALTHCARE N.V.• Belgium
GE HEALTHCARE• United States of America
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