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Centrifuge - ANVISA Registration 81246986614

Access comprehensive regulatory information for Centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81246986614 and manufactured by ORTHO CLINICAL DIAGNÓSTICS , INC.. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE 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 SORVALL, CELM COMPANHIA EQUIPADORA DE LABORATORIOS MODERNOS, 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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81246986614
Registration Details
ANVISA Registration Number: 81246986614
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Device Details

ORTHO BIOVUE SYSTEM CENTRIFUGE
Risk Class I

Registration Details

81246986614

25351455920201769

21921393000146

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2017

VIGENTE

09/18/2025 19:00:01