Lumbar decompression kit - ANVISA Registration 80981949002

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 80981949002 and manufactured by SEAWON MEDITECH CO., LTD. The registration is held by Blumedical Group Comércio de Produtos para Saúde Ltda.- ME with validity until Nov 26, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.