CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 80102513377

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 80102513377 and manufactured by AUTOBIO DIAGNOSTICS CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Feb 24, 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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80102513377
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Registration Details
ANVISA Registration Number: 80102513377
Janaina dos Santos de Miranda

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Related Devices (2)

Família AutoLumo CK-MB Micropartículas (CLIA)
Risk Class III

Registration Details

80102513377

25351413636202444

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01

Família AutoLumo CK-MB Micropartículas (CLIA)
Risk Class III

Registration Details

80102513377

25351413636202444

04718143000194

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01