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Hemodialysis Set - ANVISA Registration 80188519005

Access comprehensive regulatory information for Hemodialysis Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80188519005 and manufactured by ALLMED MIDDLE EAST. The registration is held by ALLMED PRONEFRO 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 B. BRAUN AVITUM AG, FORTECARE INDÚSTRIA DE PRODUTOS MÉDICOS 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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80188519005
Registration Details
ANVISA Registration Number: 80188519005
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Device Details

Conjunto Descartável de Circulação Assistida – Kit para hemodiálise 8mm pré-bomba 47BP+Conjunto de Tubulação para Hemodiafiltração DIALINE
Risk Class II

Registration Details

80188519005

25351449794202432

04980517000145

Company Information

ALLMED MIDDLE EAST
Egypt
PT: EGITO

Dates and Status

Dec 23, 2024

VIGENTE

09/18/2025 19:00:01