SPACER - ANVISA Registration 80203020007

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80203020007 and manufactured by manufacturer not specified. The registration is held by BONE SURGICAL EQUIPAMENTOS MEDICOS LTDA with validity until Apr 23, 2027.

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 PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA, HUIZHOU KAIYI TECHNOLOGY 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.