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

Autoclave - ANVISA Registration 80722760001

Access comprehensive regulatory information for Autoclave in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80722760001 and manufactured by AREDES EQUIPAMENTO HOSPITALARES LTDA. The registration is held by AREDES EQUIPAMENTO 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 CISABRASILE LTDA, PHOENIX LUFERCO LTDA, 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
80722760001
Registration Details
ANVISA Registration Number: 80722760001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

autoclave delta life
Risk Class II

Registration Details

80722760001

25351170748201857

09071385000152

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 11, 2019

VIGENTE

09/18/2025 19:00:01