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

Sensors - ANVISA Registration 80722809007

Access comprehensive regulatory information for Sensors in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80722809007 and manufactured by MEDKER MEDICAL ELECTRONIC TECH (SHENZHEN) CO., LTD.. The registration is held by DBI - COMÉRCIO E IMPORTAÇÃO 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 QINHUANGDAO KAPUNUOMAITE MEDICAL EQUIPMENT S AND T CO. LTD., S.L.P. LTD. SCIENTIFIC LABORATORY PRODUCTS, 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
80722809007
Registration Details
ANVISA Registration Number: 80722809007
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Eletrodo (sensor) tipo BIS marca MedPex
Risk Class II

Registration Details

80722809007

25351128301202512

07295190000160

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 01, 2025

VIGENTE

09/18/2025 19:00:01