Fistula Needle - ANVISA Registration 80567510016

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 80567510016 and manufactured by Guangdong Baihe Medical Technology Co., Ltd. The registration is held by TAUROVITA COMERCIO E IMPORTACAO LTDA 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 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.