SINGLE USE VACUUM TUBE - ANVISA Registration 10355870315

Access comprehensive regulatory information for SINGLE USE VACUUM 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 10355870315 and manufactured by Katalyst Surgical, LLC. The registration is held by BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES 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 STEMC BIYOTEKNOLOJI A.S., MED-LOGICS, INC., 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.