CA 15-3 ANTIGEN - ANVISA Registration 10033121052
Access comprehensive regulatory information for CA 15-3 ANTIGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10033121052 and manufactured by BECKMAN COULTER INC. The registration is held by BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO LTDA with validity until Sep 18, 2033.
This page provides complete technical specifications for 2 related devices, 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.
Related Devices (2)
Registration Details
10033121052
25351369295202381
42160812000144
Company Information
Dates and Status
Sep 18, 2023
18/09/2033
09/18/2025 19:00:01
ANTÍGENO CA 15-3
Família AutoLumo Micropartículas de CA15-3 (CLIA)
Not specified
80102513428
May 19, 2025
ANTÍGENO CA 15-3
Família AutoLumo Micropartículas de CA15-3 (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513428
May 19, 2025
ANTÍGENO CA 15-3
CA 15-3 Reagent Kit
LABTEST DIAGNOSTICA S/A
10009010473
Oct 21, 2024
ANTÍGENO CA 15-3
Família VITROS Immunodiagnostic Products CA 15-3 Reagent Pack and Calibrator
Not specified
81246986895
Jun 17, 2024
ANTÍGENO CA 15-3
Família VITROS Immunodiagnostic Products CA 15-3 Reagent Pack and Calibrator
ORTHO CLINICAL DIAGNOSTICS
81246986895
Jun 17, 2024

