Fistula Needle - ANVISA Registration 10390410083

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 10390410083 and manufactured by LIFEMED INDUSTRIAL DE EQUIPAMENTOS E ARTiGOS MÉDICOS E HOSPITALARES S.A. The registration is held by LIFEMED INDUSTRIAL DE EQUIPAMENTOS E ARTiGOS MÉDICOS E HOSPITALARES S.A 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.