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

Filters - ANVISA Registration 80488290009

Access comprehensive regulatory information for Filters in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80488290009 and manufactured by AG Industries/ Home Health Medical Equipment, Inc.. The registration is held by LUMIAR HEALTH BUILDERS EQUIPAMENTOS HOSPITALARES 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 INTERSURGICAL LTD., MERCK MILLIPORE LTD, 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
80488290009
Registration Details
ANVISA Registration Number: 80488290009
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Filtro Bacteriológico Lumiar
Risk Class II

Registration Details

80488290009

25351081849201487

05652247000106

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 14, 2014

VIGENTE

09/18/2025 19:00:01