Centrifuge - ANVISA Registration 80110879019

Access comprehensive regulatory information for Centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80110879019 and manufactured by SORVALL. The registration is held by SOTELAB- Sociedade Tecnica de Laboratorio Ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including CELM COMPANHIA EQUIPADORA DE LABORATORIOS MODERNOS, SORVALL, 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 Similar Products
5 Competitors
80110879019
Registration Details
ANVISA Registration Number: 80110879019
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

SORVALL WX ULTRA CENTRĂŤFUGA
Risk Class I

Registration Details

80110879019

25351761730201045

01115603000100

Company Information

SORVALL
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 07, 2011

VIGENTE

09/18/2025 19:00:01