Endobronchial Tube - ANVISA Registration 82738739003

Access comprehensive regulatory information for Endobronchial 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 82738739003 and manufactured by ROYAL FORNIA MEDICAL EQUIPMENT CO., LTD.. The registration is held by BROOK S/A 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 Hangzhou tappa medical Technology Co. Ltd., SHREE UMIYA SURGICAL PVT. 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.