CREATINE KINASE (CK) - ANVISA Registration 10377390318
Access comprehensive regulatory information for CREATINE KINASE (CK) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10377390318 and manufactured by KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA. The registration is held by KATAL BIOTECNOLOGICA INDUSTRIA E COMERCIO LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including GOLD ANALISA DIAGNOSTICA LTDA, ROCHE DIAGNOSTICS GMBH, 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
10377390318
25351071148202536
71437917000104
Company Information
Dates and Status
Jun 02, 2025
VIGENTE
09/18/2025 19:00:01
CREATINOQUINASE (CK)
Família CK NAC
GOLD ANALISA DIAGNOSTICA LTDA
80022230299
Aug 18, 2025
CREATINOQUINASE (CK)
CK NAC Automação - Linha DT
DAILYTECH LATINO AMERICA LTDA
80657030079
Apr 07, 2025
CREATINOQUINASE (CK)
CK-NAC
IN VITRO DIAGNOSTICA LTDA
10303460560
Mar 17, 2025
CREATINOQUINASE (CK)
CK (W) Simplex
TASCOM CO., LTD
80074330020
Feb 17, 2025
CREATINOQUINASE (CK)
CK Simplex
TASCOM CO., LTD
80074330007
Jan 06, 2025

