Laryngeal Tube - ANVISA Registration 82059269020

Access comprehensive regulatory information for Laryngeal 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 82059269020 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 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.