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MALONDIALDEHYDE - ANVISA Registration 80464810822

Access comprehensive regulatory information for MALONDIALDEHYDE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810822 and manufactured by LUMIQUICK DIAGNOSTICS, INC.. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including IMMUNDIAGNOSTIK AG, CHUNGDO PHARM CO., LTD., and 3 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.

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80464810822
Registration Details
ANVISA Registration Number: 80464810822
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Device Details

QuickProfileTM OxiStressTM MDA-586 Assay Kit
Risk Class II

Registration Details

80464810822

25351194508202313

09377976000152

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 02, 2023

VIGENTE

09/18/2025 19:00:01

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