GLUTATHIONE PEROXIDASE - ANVISA Registration 80158990139
Access comprehensive regulatory information for GLUTATHIONE PEROXIDASE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80158990139 and manufactured by RANDOX LABORATORIES LTD.. The registration is held by RANDOX BRASIL LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including RANDOX LABORATORIES LTD., LUMIQUICK DIAGNOSTICS, INC., and 4 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
80158990139
25351346404201068
05257628000190
Company Information
Dates and Status
Jan 10, 2011
VIGENTE
09/18/2025 19:00:01
GLUTATIONA PEROXIDASE
CALIBRADOR RANSEL
RANDOX LABORATORIES LTD
80158990321
Dec 23, 2024
GLUTATIONA PEROXIDASE
OxiStressโข GSH/GSSG-412 Assay Kit
LUMIQUICK DIAGNOSTICS, INC.
80464810821
May 02, 2023
GLUTATIONA PEROXIDASE
GLUTATIONA REDUTASE
RANDOX LABORATORIES LTD.
80158990278
Nov 28, 2016
GLUTATIONA PEROXIDASE
CONTROLE RANSEL
RANDOX LABORATORIES LTD.
80158990200
Feb 02, 2015

