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

Humidifier - ANVISA Registration 10317700020

Access comprehensive regulatory information for Humidifier in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10317700020 and manufactured by SALTER LABS. The registration is held by SOLDAGÁS COMÉRCIO DE GASES E SOLDAS 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 PULMODYNE, INC, FISHER & PAYKEL HEALTHCARE LIMITED, 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
10317700020
Registration Details
ANVISA Registration Number: 10317700020
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

UMIDIFICADOR SALTER LABS
Risk Class II

Registration Details

10317700020

25351209822201788

91668137000174

Company Information

SALTER LABS
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 22, 2017

VIGENTE

09/18/2025 19:00:01