Electrical Stimulator - ANVISA Registration 82073819001
Access comprehensive regulatory information for Electrical Stimulator in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82073819001 and manufactured by JOYLUX, INC.. The registration is held by ESSITY DO BRASIL IND. E COMÉRCIO 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 NKL PRODUTOS ELETRÔNICOS LTDA - EPP, DGM ELETRÔNICA LTDA-EPP, 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.
Device Details
Registration Details
82073819001
25351387224202441
72899016000512
Company Information
Dates and Status
Oct 29, 2024
VIGENTE
09/18/2025 19:00:01
Estimulador Eletrico
LIFTRON
DGM ELETRÔNICA LTDA-EPP
80108309003
Sep 09, 2024
Estimulador Eletrico
Dispositivo de Biofeedback Eletromiográfico (EMG)
VERITY MEDICAL LTD.
80633669005
Aug 05, 2024
Estimulador Eletrico
Dispositivo de Eletroterapia
VERITY MEDICAL LTD.
80633669006
Aug 05, 2024
Estimulador Eletrico
Estimulador de Eletroterapia Transcraniana
NEXALIN TECHNOLOGY INCORPORATED
80102519252
May 28, 2024
Estimulador Eletrico
Eletroestimulador EL30 - NKL
NKL PRODUTOS ELETRÔNICOS LTDA - EPP
80191689005
Sep 18, 2023

