Electromagnetic Equipment for Therapy - ANVISA Registration 81022039005

Access comprehensive regulatory information for Electromagnetic Equipment for Therapy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81022039005 and manufactured by SPRINGLIFE MEDICAL B.V.. The registration is held by SOLLIEVO MEDICINA ESPECIALIZADA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including NEUROSOFT LTD, BIOMAG MEDICAL S.R.O, 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.