Endobronchial Tube - ANVISA Registration 82059269015

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 82059269015 and manufactured by NINGBO MFLAB (YINDONG) MEDICAL INSTRUMENTS CO., LTD. The registration is held by DLM HOSPITALAR 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 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.