Lumbar decompression kit - ANVISA Registration 81288540040

Access comprehensive regulatory information for Lumbar decompression kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81288540040 and manufactured by HORTRON INDUSTRIA E COMERCIO DE PRODUTOS ELETRONICOS LTDA - ME. The registration is held by Hortron Indústria e Comercio de Produtos Eletrônicos LTDA-ME with validity until Jun 13, 2032.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME, MARDEN MEDICAL LTDA, 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.