Tubes - ANVISA Registration 81612410008

Access comprehensive regulatory information for Tubes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81612410008 and manufactured by PROMEPLA S.A.M. The registration is held by ERBE DO BRASIL EQUIPAMENTOS CIRURGICOS E ENDOSCOPICOS 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 RICHARD WOLF GMBH, BIOVICO SP. Z O.O., 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.