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

Flowmeter - ANVISA Registration 81278590033

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 81278590033 and manufactured by NINGBO YINZHOU XIANFENG ELECTRONICS INSTRUMENT FACTORY. 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 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81278590033
Registration Details
ANVISA Registration Number: 81278590033
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Fluxômetro para Oxigêncio - Gaslive
Risk Class I

Registration Details

81278590033

25351020987202243

16686026000175

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 27, 2022

VIGENTE

09/18/2025 19:00:01