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.
Related Devices (2)
Registration Details
80615950231
25351373252201914
09322796000173
Company Information
Dates and Status
Aug 19, 2019
19/08/2029
09/18/2025 19:00:01
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
BIOCLIN POCT FIA CK-MB
QUIBASA QUÍMICA BÁSICA LTDA
10269360481
Sep 15, 2025
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Luminis FIA CK-MB
Not specified
80474870168
Sep 08, 2025
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Luminis FIA CK-MB
QINGDAO HIGHTOP BIOTECH CO.,LTD.
80474870168
Sep 08, 2025
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Família Soro Controle CK-MB
BIOSYSTEMS S.A.
80367750195
Jul 28, 2025
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Família Soro Controle CK-MB
Not specified
80367750195
Jul 28, 2025

