Extension Tube - ANVISA Registration 81056910003

Access comprehensive regulatory information for Extension Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81056910003 and manufactured by NEOFLEX BIOTECNOLOGIA LTDA - ME. The registration is held by NEOFLEX BIOTECNOLOGIA LTDA - ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including M P - COMERCIO E INDUSTRIA DE MATERIAIS HOSPITALARES LTDA, HARTMANN IND COM PRODS MEDICO HOSPITALARES LTDA, 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.