CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 81246982501

Access comprehensive regulatory information for CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246982501 and manufactured by ORTHO CLINICAL DIAGNOSTICS, INC. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Dec 19, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, SIEMENS HEALTHCARE DIAGNOSTICS 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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81246982501
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Registration Details
ANVISA Registration Number: 81246982501
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

VERIFICADOR DE EFICIENCIA ISOENZIMA I E II VITROS*
Risk Class III

Registration Details

81246982501

25351455780201729

21921393000146

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2017

19/12/2026

09/18/2025 19:00:01

VERIFICADOR DE EFICIENCIA ISOENZIMA I E II VITROS*
Risk Class III

Registration Details

81246982501

25351455780201729

21921393000146

Dates and Status

Aug 28, 2017

19/12/2026

09/18/2025 19:00:01