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Software - ANVISA Registration 80733809002

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 80733809002 and manufactured by NEOLOGICA S.R.L.. The registration is held by PENTA TECHNOLOGIES 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 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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80733809002
Registration Details
ANVISA Registration Number: 80733809002
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Device Details

DICOMJet
Risk Class I

Registration Details

80733809002

25351279996201268

08241634000148

Company Information

NEOLOGICA S.R.L.
Italy
PT: ITรLIA

Dates and Status

Sep 17, 2012

VIGENTE

09/18/2025 19:00:01