Fistula Needle - ANVISA Registration 80188510034

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 80188510034 and manufactured by ALLMED MIDDLE EAST. The registration is held by ALLMED PRONEFRO BRASIL 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 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.