Electromyographic endotracheal tube electrode - ANVISA Registration 81704069039

Access comprehensive regulatory information for Electromyographic endotracheal tube electrode in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81704069039 and manufactured by EVO MEDICINA ESPECIALIZADA LTDA. The registration is held by EVO MEDICINA ESPECIALIZADA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MIT MEDICAL INDUSTRY TECHNOLOGY LTDA - ME, STARMEDIX INDUSTRIA E COMÉRCIO DE EQUIPAMENTOS MÉDICOS E ODONTOLÓGICOS 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 Similar Products
5 Competitors
81704069039
Registration Details
ANVISA Registration Number: 81704069039
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

Kit Tubo Endotraqueal e Eletrodo de Laringe Adesivo EVO
Risk Class II

Registration Details

81704069039

25351453986202443

14021783000102

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 10, 2025

VIGENTE

09/18/2025 19:00:01