SPACER FOR OTORHINOLARYNGOLOGY - ANVISA Registration 82530260005

Access comprehensive regulatory information for SPACER FOR OTORHINOLARYNGOLOGY in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82530260005 and manufactured by OSCIMED SA. The registration is held by LONGEVICORP S.A with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including CIPLA LIMITED, and 1 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.