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ERYTHROCYTE SEDIMENTATION RATE (ESR) - ANVISA Registration 80020690240

Access comprehensive regulatory information for ERYTHROCYTE SEDIMENTATION RATE (ESR) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80020690240 and manufactured by BIO - RAD LABORATORIES. The registration is held by BIO-RAD LABORATORIOS 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 DIESSE DIAGNÓSTICA SENESE S.P.A, ALCOR SCIENTIFIC INC., 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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80020690240
Registration Details
ANVISA Registration Number: 80020690240
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Device Details

Família Liquichek Sedimentation Rate Control
Risk Class II

Registration Details

80020690240

25351088306201028

03188198000177

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 13, 2010

VIGENTE

09/18/2025 19:00:01