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CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 80615950231

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 80615950231 and manufactured by HUMASIS CO., LTDA. The registration is held by Diagmaster Científica ltda with validity until Aug 19, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80615950231
2 Related Devices
Registration Details
ANVISA Registration Number: 80615950231
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Related Devices (2)

Registration Details

80615950231

25351373252201914

09322796000173

Company Information

HUMASIS CO., LTDA
South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 19, 2019

19/08/2029

09/18/2025 19:00:01

Registration Details

80615950231

25351373252201914

09322796000173

Company Information

Dates and Status

Aug 19, 2019

19/08/2029

09/18/2025 19:00:01