IMMUNOHEMATOLOGY - RED BLOOD CELL REAGENTS/ENZYME-TREATED RED BLOOD CELL REAGENTS - ANVISA Registration 80134860300
Access comprehensive regulatory information for IMMUNOHEMATOLOGY - RED BLOOD CELL REAGENTS/ENZYME-TREATED RED BLOOD CELL REAGENTS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80134860300 and manufactured by manufacturer not specified. The registration is held by GRIFOLS BRASIL LTDA with validity until Oct 23, 2033.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including IMMUCOR, INC, MEDION DIAGNOSTICS GRIFOLS AG, 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
80134860300
25351019422202302
02513899000171
Company Information
Dates and Status
Oct 23, 2023
23/10/2033
09/18/2025 19:00:01
IMUNOHEMATOLOGIA - REAGENTES DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
FAMÍLIA REAGENTE DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
BIO-RAD LABORATORIOS BRASIL LTDA.
80020690461
Jul 14, 2025
IMUNOHEMATOLOGIA - REAGENTES DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
Screen-Cyte Dia 3%
MEDION DIAGNOSTICS GRIFOLS AG
80134860297
Oct 23, 2023
IMUNOHEMATOLOGIA - REAGENTES DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
Screen-Cyte Dia 3%
Not specified
80134860297
Oct 23, 2023
IMUNOHEMATOLOGIA - REAGENTES DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
Sero-Cyte 3%
MEDION DIAGNOSTICS GRIFOLS AG
80134860299
Oct 23, 2023
IMUNOHEMATOLOGIA - REAGENTES DE HEMÁCIAS/DE HEMÁCIAS TRATADAS COM ENZIMAS
Sero-Cyte 3%
Not specified
80134860299
Oct 23, 2023

