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 80352500022

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 80352500022 and manufactured by EURONDA - SPA. The registration is held by BOMA COMÉRCIO 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
80352500022
Registration Details
ANVISA Registration Number: 80352500022
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

AUTOCLAVE EURONDA PRO SYSTEM
Risk Class II

Registration Details

80352500022

25351476974202144

05167642000101

Company Information

EURONDA - SPA
Italy
PT: ITÁLIA

Dates and Status

Nov 04, 2021

VIGENTE

09/18/2025 19:00:01