ANTI-HUMAN GLOBULIN (COOMBS) - ANVISA Registration 10154450180
Access comprehensive regulatory information for ANTI-HUMAN GLOBULIN (COOMBS) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10154450180 and manufactured by FRESENIUS HEMOCARE BRASIL LTDA.. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until Nov 27, 2027.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DIAMED GMBH, ORTHO CLINICAL DIAGNOSTICS, 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
10154450180
25351365385201757
49601107000184
Company Information
Dates and Status
Nov 27, 2017
27/11/2027
09/18/2025 19:00:01
GLOBULINA ANTI-HUMANA (COOMBS)
ID-DC Screening II
Not specified
80020690455
Jul 14, 2025
GLOBULINA ANTI-HUMANA (COOMBS)
ID-Coombs Anti-IgG
Not specified
80020690463
Jul 14, 2025
GLOBULINA ANTI-HUMANA (COOMBS)
ID-DC Screening II
DIAMED GMBH
80020690455
Jul 14, 2025
GLOBULINA ANTI-HUMANA (COOMBS)
ID-DAT IgG - Dilution
Not specified
80020690462
Jul 14, 2025
GLOBULINA ANTI-HUMANA (COOMBS)
ID-DAT IgG1/IgG3
DIAMED GMBH
80020690454
Jul 14, 2025

