CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 10269360481
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 10269360481 and manufactured by QUIBASA QUÍMICA BÁSICA LTDA. The registration is held by QUIBASA - QUIMICA BASICA LTDA with validity until Sep 15, 2035.
This page provides complete technical specifications for this device, 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.
Device Details
Registration Details
10269360481
25351099507202510
19400787000107
Company Information
Dates and Status
Sep 15, 2025
15/09/2035
09/18/2025 19:00:01
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
CREATINOQUINASE ISOENZIMAS (CKMB, CKBB, CKMM)
Teste Rápido CK-MB
Not specified
81472060043
May 26, 2025

