BIOPSY NEEDLE - ANVISA Registration 82592939008

Access comprehensive regulatory information for BIOPSY NEEDLE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82592939008 and manufactured by VITROLIFE SWEDEN AB. The registration is held by Intermariner do Brasil Comercio, Importação e Exportação 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 STERYLAB S.R.L., ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., 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.