CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 10345160052

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 10345160052 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Jan 12, 2028.

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, BIOSYSTEMS S.A., 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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10345160052
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Registration Details
ANVISA Registration Number: 10345160052
Janaina dos Santos de Miranda

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Related Devices (2)

CAL CKMB CALIBRATOR ADVIA CENTAUR ACS: 180 SYSTEMS
Risk Class III

Registration Details

10345160052

250000293239711

01449930000190

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 12, 1998

12/01/2028

09/18/2025 19:00:01

CAL CKMB CALIBRATOR ADVIA CENTAUR ACS: 180 SYSTEMS
Risk Class III

Registration Details

10345160052

250000293239711

01449930000190

Company Information

Dates and Status

Jan 12, 1998

12/01/2028

09/18/2025 19:00:01