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

Respiratory Exerciser - ANVISA Registration 81001390003

Access comprehensive regulatory information for Respiratory Exerciser in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81001390003 and manufactured by POWERBREATHE INTERNATIONAL LTD.. The registration is held by HAB AMERICA DO SUL COMERCIO IMPORTAÇÃO E EXPORTAÇÃO DE EQUIPAMENTOS LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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
81001390003
Registration Details
ANVISA Registration Number: 81001390003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

POWERBREATHE APARELHO PARA FISIOTERAPIA RESPIRATORIA
Risk Class I

Registration Details

81001390003

25351115273201917

16586751000171

Company Information

England (United Kingdom)
PT: INGLATERRA (REINO UNIDO)

Dates and Status

May 08, 2019

VIGENTE

09/18/2025 19:00:01