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

Oral Humidifier - ANVISA Registration 81008610002

Access comprehensive regulatory information for Oral Humidifier in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81008610002 and manufactured by LIFESTREAM PHARMA. The registration is held by FNL COMÉRCIO DE SUPRIMENTOS 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 MEGALABS FARMACEUTICA S.A., LIFESTREAM PHARMA NV, 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
81008610002
Registration Details
ANVISA Registration Number: 81008610002
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

BIOXTRA DRY MOUTH MILD MOUTHRINSE
Risk Class I

Registration Details

81008610002

25351183446201920

03439555000122

Company Information

LIFESTREAM PHARMA
Belgium
PT: BÉLGICA

Dates and Status

May 08, 2019

VIGENTE

09/18/2025 19:00:01