SPACER - ANVISA Registration 81596320085

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81596320085 and manufactured by SHENZHEN HOMED MEDICAL DEVICE CO., LTD.. The registration is held by MULTILASER INDUSTRIAL S.A. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, 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.