Fistula Needle - ANVISA Registration 80808480030

Access comprehensive regulatory information for Fistula 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 80808480030 and manufactured by SHANGHAI MEKON MEDICAL DEVICES CO., LTD.. The registration is held by BECARE COMÉRCIO DE PRODUTOS MÉDICO HOSPITALARES LTDA EPP 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 BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD, BIOTEQUE CORPORATION, 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.