Electrical Stimulator - ANVISA Registration 80191689004
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 80191689004 and manufactured by NKL PRODUTOS ELETRÔNICOS LTDA - EPP. The registration is held by NKL PRODUTOS ELETRÔNICOS LTDA - EPP 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 DGM ELETRÔNICA LTDA-EPP, IBRAMED INDÚSTRIA BRASILEIRA DE EQUIPAMENTOS MÉDICOS - LTDA, 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
80191689004
25351171795202385
04920239000130
Company Information
Dates and Status
Apr 17, 2023
VIGENTE
09/18/2025 19:00:01
Estimulador Eletrico
APARELHO PARA ESTIMULAÇÃO PÉLVICA ISSVIVA
JOYLUX, INC.
82073819001
Oct 29, 2024
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

