Pure Global

EEG Monitor - ANVISA Registration 80386680011

Access comprehensive regulatory information for EEG Monitor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80386680011 and manufactured by CADWELL INDUSTRIES, INC.. The registration is held by med 7 produtos hospitalares ltda epp with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including DANMETER A/S, FRESENIUS KABI AG, and 2 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
2 Competitors
2 Recent Registrations
80386680011
Registration Details
ANVISA Registration Number: 80386680011
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

IOMAX CASCADE
Risk Class II

Registration Details

80386680011

25351588539202081

08140941000132

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Jul 06, 2020

VIGENTE

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "EEG Monitor"