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ANVISA registration 80188519007Active

Tube For Extracorporeal Circulation

ANVISA Registration Number: 80188519007ALLMED PRONEFRO BRASIL LTDAALLMED MIDDLE EASTRisk Class II
Verified
Device names
Technical name
Tube For Extracorporeal Circulation
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PT: Tubo Para Circulacao Extracorporea
Commercial name
Conjunto Descartável de Circulação Assistida – Acessório para linha de sangue para transporte de sangue arterial em terapia de hemodiálise HDF
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Risk class
Class II
Registration details
Registration Number
80188519007
Process Number
25351450223202441
CNPJ
04980517000145
Company information
Registration Holder
ALLMED PRONEFRO BRASIL LTDA
Manufacturer
ALLMED MIDDLE EAST
Manufacturing Country
Egypt
PT: EGITO
Dates and status
Publication Date
Dec 23, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Tube For Extracorporeal Circulation in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80188519007 and manufactured by ALLMED MIDDLE EAST. The registration is held by ALLMED PRONEFRO BRASIL LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.