Bi-Level CPAP - ANVISA Registration 80047300521

Access comprehensive regulatory information for Bi-Level CPAP in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80047300521 and manufactured by RESMED PTY LTD.. The registration is held by MEDSTAR IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SUZHOU YUYUE MEDICAL TECHNOLOGY CO. LTD., CMOS DRAKE S.A, 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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80047300521
Registration Details
ANVISA Registration Number: 80047300521
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

GERADOR DE FLUXO PARA TERAPIA RESPIRATÓRIA
Risk Class II

Registration Details

80047300521

25351272439201406

03580620000135

Company Information

RESMED PTY LTD.
Australia
PT: AUSTRÁLIA

Dates and Status

Sep 22, 2014

VIGENTE

09/18/2025 19:00:01