Blood bank centrifuge - ANVISA Registration 80110879022

Access comprehensive regulatory information for Blood bank centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80110879022 and manufactured by QINGDAO HAIER BIOMEDICAL CO., LTD.. 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, 1 companies making the same product including FRESENIUS KABI AG, and 1 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.