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BLOOD GASES - ANVISA Registration 81246980019

Access comprehensive regulatory information for BLOOD GASES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246980019 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Aug 25, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 companies making the same product including BIO-RAD LABORATORIES INC, ROCHE DIAGNOSTICS GMBH, 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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81246980019
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Registration Details
ANVISA Registration Number: 81246980019
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Related Devices (2)

REATIVO SECO VITROS* DIOXIDO DE CARBONO ENZIMATICOECO2
Risk Class III

Registration Details

81246980019

25351455317201787

21921393000146

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2017

25/08/2035

09/18/2025 19:00:01

REATIVO SECO VITROS* DIOXIDO DE CARBONO ENZIMATICOECO2
Risk Class III

Registration Details

81246980019

25351455317201787

21921393000146

Dates and Status

Aug 28, 2017

25/08/2035

09/18/2025 19:00:01