Laryngeal Tube - ANVISA Registration 80102511683

Access comprehensive regulatory information for Laryngeal Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80102511683 and manufactured by AIRLIFE. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including HANGZHOU TRIFANZ MEDICAL DEVICE CO.LTD., INTERSURGICAL LTD., 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.