Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Oxygenators - ANVISA Registration 80259119029

Access comprehensive regulatory information for Oxygenators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80259119029 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 TERUMO CORPORATION, BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80259119029
Registration Details
ANVISA Registration Number: 80259119029
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit VKMO Iberia 11000 - Oxigenador de Membrana Quadrox-i Neonatal com Filtro Arterial e Reservatรณrio de Cardiotomia
Risk Class II

Registration Details

80259119029

25351462228202335

06028137000130

Company Information

Germany
PT: ALEMANHA

Dates and Status

Aug 28, 2023

VIGENTE

09/18/2025 19:00:01