BIOPSY NEEDLE - ANVISA Registration 80991389030

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 80991389030 and manufactured by KFF S.A.. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO 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.