Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

NITRITE - ANVISA Registration 80464810829

Access comprehensive regulatory information for NITRITE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810829 and manufactured by LUMIQUICK DIAGNOSTICS, INC.. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATร“RIOS 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 CHUNGDO PHARM CO., LTD., IMMUNDIAGNOSTIK AG, and 2 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
2 Competitors
2 Recent Registrations
80464810829
Registration Details
ANVISA Registration Number: 80464810829
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

QuickProfileTM OxiStressTM Nitric Oxide Enzymatic Assay Kit
Risk Class II

Registration Details

80464810829

25351264207202356

09377976000152

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

May 29, 2023

VIGENTE

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "NITRITE"