FIBRINOGEN - ANVISA Registration 10269360446
Access comprehensive regulatory information for FIBRINOGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10269360446 and manufactured by QUIBASA QUÍMICA BÁSICA LTDA. The registration is held by QUIBASA - QUIMICA BASICA 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 BIOSYSTEMS S.A., 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
10269360446
25351897914202412
19400787000107
Company Information
Dates and Status
Jan 22, 2024
VIGENTE
09/18/2025 19:00:01
FIBRINOGÊNIO
Dia-FIB
DIAGON KFT.
80019640095
Mar 05, 2025
FIBRINOGÊNIO
Kit de Teste de Fibrinogênio (Método de Clauss Modificado)
SHENZHEN DYMIND BIOTECHNOLOGY CO., LTD
82444370184
Jan 27, 2025
FIBRINOGÊNIO
Calibrador de Fibrinogênio
SHENZHEN DYMIND BIOTECHNOLOGY CO., LTD
82444370147
Oct 07, 2024
FIBRINOGÊNIO
EBCOAG FIB - Fibrinogênio
EBRAM PRODUTOS LABORATORIAIS LTDA
10159820262
Sep 09, 2024
FIBRINOGÊNIO
STA – Liquid FIB
DIAGNOSTICA STAGO S.A.S
81457600055
Sep 25, 2023

