ALPHA 1-ACID GLYCOPROTEIN (AGP) - ANVISA Registration 80367750133
Access comprehensive regulatory information for ALPHA 1-ACID GLYCOPROTEIN (AGP) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80367750133 and manufactured by BIOSYSTEMS S.A.. The registration is held by BIOSYSTEMS NE COMÉRCIO DE PRODUTOS LABORATORIAIS E HOSPITALARES 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 QUIBASA QUÍMICA BÁSICA LTDA, 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
80367750133
25351042795202298
08282077000103
Company Information
Dates and Status
Jun 09, 2022
VIGENTE
09/18/2025 19:00:01
ALFA 1-GLICOPROTEÍNA ÁCIDA (AGPA)
Família AAG
KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA
10377390275
Feb 17, 2025
ALFA 1-GLICOPROTEÍNA ÁCIDA (AGPA)
ALFA - 1 - GLICOPROTEÍNA ÁCIDA BA400
BIOSYSTEMS S.A.
80367750103
Sep 14, 2020
ALFA 1-GLICOPROTEÍNA ÁCIDA (AGPA)
Alfa 1 Glicoproteína Ácida
VYTTRA DIAGNOSTICOS S.A.
81692610186
Sep 08, 2020
ALFA 1-GLICOPROTEÍNA ÁCIDA (AGPA)
AAGP2 (Tina-quant a1-Acid Glycoprotein Gen.)_cobas c
ROCHE DIAGNOSTICS GMBH
10287411459
Dec 23, 2019
ALFA 1-GLICOPROTEÍNA ÁCIDA (AGPA)
Alinity c A-1-AGP Reagent Kit
BIOKIT, S.A.
80146502235
Nov 18, 2019

