CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 81325990187

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 81325990187 and manufactured by ACRO BIOTECH, INC. (MONTCLAIR). The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until May 24, 2031.

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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81325990187
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Registration Details
ANVISA Registration Number: 81325990187
Janaina dos Santos de Miranda

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Related Devices (2)

FamĂ­lia Cassete de teste para CK-MB ( Sangue total/Soro/Plasma)
Risk Class III

Registration Details

81325990187

25351232753202166

19933144000129

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 24, 2021

24/05/2031

09/18/2025 19:00:01

FamĂ­lia Cassete de teste para CK-MB ( Sangue total/Soro/Plasma)
Risk Class III

Registration Details

81325990187

25351232753202166

19933144000129

Dates and Status

May 24, 2021

24/05/2031

09/18/2025 19:00:01