Non-thermal plasma wound therapy system - ANVISA Registration 82071039002

Access comprehensive regulatory information for Non-thermal plasma wound therapy system in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82071039002 and manufactured by TERRAPLASMA MEDICAL GMBH. The registration is held by PROMEDIOL DO BRASIL LTDA 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, 3 companies making the same product including SURFACE MEDICA - EQUIPAMENTOS ELETRONICOS LTDA, FEAGLE CORPORATION, and 4 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.