ANVISA registration
Gerador de Fluxo para Terapia Respiratória Resmed - Série Air 11
Registration 82507529004. Unidade CPAP doméstica
Registration details
| Registration number | 82507529004 |
|---|---|
| Application number | 25351086494202519 |
| Technical name | Unidade CPAP doméstica |
| Risk class | II |
| Published on | 30/06/2025 |
| Validity | Indefinite validity |
Registration holder
| Legal name | RESMED BRASIL REPRESENTAÇÕES DE PRODUTOS MÉDICOS LTDA. |
|---|---|
| CNPJ | 07.733.293/0001-65 |
Manufacturer
- RESMED PTY LTD. AUSTRÁLIA
Other registrations held by RESMED BRASIL REPRESENTAÇÕES DE PRODUTOS MÉDICOS LTDA.view all
Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
Next step
Medical device registration with ANVISA
HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.
Speak to a specialist