Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Electrical Stimulator - ANVISA Registration 81979130000

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 81979130000 and manufactured by DOMINO S.R.L.. The registration is held by GLOBUS BRASIL HI TECH COMERCIO DE EQUIPAMENTOS IMPORTACAO E EXPORTACAO 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81979130000
Registration Details
ANVISA Registration Number: 81979130000
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

GENESY 1200 PRO
Risk Class II

Registration Details

81979130000

25351396617202012

13480805000202

Company Information

DOMINO S.R.L.
Italy
PT: ITÁLIA

Dates and Status

Jun 29, 2020

VIGENTE

09/18/2025 19:00:01