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

Monitoring Kit - ANVISA Registration 80969869013

Access comprehensive regulatory information for Monitoring Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80969869013 and manufactured by SHENZHEN SINELINK ELECTRONICS CO., LTD. The registration is held by AS2 COMERCIO IMPORTACAO E EXPORTACAO 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 EDWARDS LIFESCIENCES LLC (IRVINE, CA), NEURO TECNOLOGIA DA AMERICA LATINA IMPORTAÇÃO E EXPORTAÇÃO 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
80969869013
Registration Details
ANVISA Registration Number: 80969869013
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT CÂNULA PARA NEUROMONITORIZAÇÃO NEUROSIGN V4 - FACIAL
Risk Class II

Registration Details

80969869013

25351041201202574

13598814000111

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 14, 2025

VIGENTE

09/18/2025 19:00:01