Tracheal Tube - ANVISA Registration 81521809001

Access comprehensive regulatory information for Tracheal 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 81521809001 and manufactured by GUANGZHOU AMK MEDICAL EQUIPMENT CO., LTD.. The registration is held by BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME 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 ZHANJIANG STAR ENTERPRISE CO,.LTD, HANGZHOU FORMED MEDICAL DEVICES CO., 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.