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CENTRIFUGAL PUMP FOR CARDIOPULMONARY BYPASS SYSTEM - ANVISA Registration 10159039003

Access comprehensive regulatory information for CENTRIFUGAL PUMP FOR CARDIOPULMONARY BYPASS SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10159039003 and manufactured by BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA. The registration is held by BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA, LIVANOVA DEUTSCHLAND GMBH, 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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10159039003
Registration Details
ANVISA Registration Number: 10159039003
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Device Details

Bomba Centrífuga Safira Centriflux® com revestimento BRCoating®
Risk Class II

Registration Details

10159039003

25351421147202032

52828936000109

Company Information

Dates and Status

Dec 03, 2020

VIGENTE

09/18/2025 19:00:01