TOXOPLASMA GONDII - ANVISA Registration 10269360467
Access comprehensive regulatory information for TOXOPLASMA GONDII in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10269360467 and manufactured by QUIBASA QUÍMICA BÁSICA LTDA. The registration is held by QUIBASA - QUIMICA BASICA LTDA with validity until Jun 09, 2035.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ABBOTT GMBH, 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
10269360467
25351018157202507
19400787000107
Company Information
Dates and Status
Jun 09, 2025
09/06/2035
09/18/2025 19:00:01
TOXOPLASMA GONDII
Família MAGLUMI IgG de Toxoplasmose (CLIA)
Not specified
80102513489
Jul 28, 2025
TOXOPLASMA GONDII
Família MAGLUMI IgG de Toxoplasmose (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102513489
Jul 28, 2025
TOXOPLASMA GONDII
IMUNOSCREEN TOXOPLASMOSE IGG DBS
MBIOLOG DIAGNOSTICOS LTDA
80047580228
Jul 14, 2025
TOXOPLASMA GONDII
BIOLISA TOXOPLASMOSE IgM
QUIBASA QUÍMICA BÁSICA LTDA
10269360466
Jun 09, 2025
TOXOPLASMA GONDII
Família VITROS Immunodiagnostic Products Toxoplasma IgM Reagent and Calibrator
ORTHO CLINICAL DIAGNOSTICS
81246986906
May 19, 2025

