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Centrifugal Pump - ANVISA Registration 80259110225

Access comprehensive regulatory information for Centrifugal Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80259110225 and manufactured by MAQUET CARDIOPULMONARY GMBH. The registration is held by GETINGE DO BRASIL EQUIPAMENTOS MEDICOS 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 INTERNATIONAL BIOPHYSICS CO, TERUMO CARDIOVASCULAR SYSTEM CORPORATION, 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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80259110225
Registration Details
ANVISA Registration Number: 80259110225
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Device Details

Bomba Centrรญfuga RF-32
Risk Class II

Registration Details

80259110225

25351385009202082

06028137000130

Company Information

Germany
PT: ALEMANHA

Dates and Status

May 18, 2020

VIGENTE

09/18/2025 19:00:01