Home CPAP unit - ANVISA Registration 82507529004

Access comprehensive regulatory information for Home CPAP unit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82507529004 and manufactured by RESMED PTY LTD.. The registration is held by RESMED BRASIL REPRESENTAÇÕES DE PRODUTOS MÉDICOS 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, 2 companies making the same product including SUZHOU YUYUE MEDICAL TECHNOLOGY CO. LTD., MICOMME MEDICAL TECHNOLOGY DEVELOPMENT CO., LTD., and 4 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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82507529004
Registration Details
ANVISA Registration Number: 82507529004
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Gerador de Fluxo para Terapia Respiratória Resmed - Série Air 11
Risk Class II

Registration Details

82507529004

25351086494202519

07733293000165

Company Information

RESMED PTY LTD.
Australia
PT: AUSTRÁLIA

Dates and Status

Jun 30, 2025

VIGENTE

09/18/2025 19:00:01

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