Lumbar decompression kit - ANVISA Registration 81130100052

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 81130100052 and manufactured by VOLMED BRASIL EQUIPAMENTOS LTDA - ME. The registration is held by VOLMED BRASIL EQUIPAMENTOS LTDA - ME with validity until Sep 02, 2034.

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.