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Flowmeter - ANVISA Registration 80171530106

Access comprehensive regulatory information for Flowmeter in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80171530106 and manufactured by MAXTEC LLC.. The registration is held by MAKE LINE COMERCIAL LTDA ME 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 JG MORIYA REPRESENTAÇÃO IMPORTADORA EXPORTADORA COMERCIAL LTDA, UNITEC INDUSTRIA E COMERCIO DE APARELHOS HOSPITALARES LTDA, 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.

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80171530106
Registration Details
ANVISA Registration Number: 80171530106
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Device Details

Misturador de Ar/O2 MaxFlo Mini
Risk Class I

Registration Details

80171530106

25351478671201941

05416754000140

Company Information

MAXTEC LLC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 29, 2019

VIGENTE

09/18/2025 19:00:01