CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 80146501214

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 80146501214 and manufactured by ABBOTT IRELAND DIAGNOSTIC DIVISION. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Feb 22, 2035.

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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80146501214
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Registration Details
ANVISA Registration Number: 80146501214
Janaina dos Santos de Miranda

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Related Devices (2)

ARCHITECT STAT CK-MB CALIBRATOR / ARCHITECT STAT CK-MB CALIBRADOR
Risk Class III

Registration Details

80146501214

25351256232200401

56998701000116

Company Information

Ireland
PT: IRLANDA

Dates and Status

Feb 22, 2005

22/02/2035

09/18/2025 19:00:01

ARCHITECT STAT CK-MB CALIBRATOR / ARCHITECT STAT CK-MB CALIBRADOR
Risk Class III

Registration Details

80146501214

25351256232200401

56998701000116

Company Information

Dates and Status

Feb 22, 2005

22/02/2035

09/18/2025 19:00:01