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 80108309003

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 80108309003 and manufactured by DGM ELETRÔNICA LTDA-EPP. The registration is held by DGM Eletrônica 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 NKL PRODUTOS ELETRÔNICOS 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80108309003
Registration Details
ANVISA Registration Number: 80108309003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

80108309003

25351374081202416

02132663000195

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 09, 2024

VIGENTE

09/18/2025 19:00:01