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Flowmeter - ANVISA Registration 81278590002

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 81278590002 and manufactured by Acare Technology Co., Ltd.. The registration is held by GASLIVE IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, 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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81278590002
2 Related Devices
Registration Details
ANVISA Registration Number: 81278590002
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Related Devices (2)

Regulador de Pressão Medicinal com Fluxômetro
Risk Class I

Registration Details

81278590002

25351826722201680

16686026000175

Company Information

Taiwan
PT: TAIWAN

Dates and Status

Apr 25, 2016

VIGENTE

09/18/2025 19:00:01

Regulador de Pressão Medicinal com Fluxômetro
Risk Class I

Registration Details

81278590002

25351826722201680

16686026000175

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 25, 2016

VIGENTE

09/18/2025 19:00:01