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Monitoring Kit - ANVISA Registration 80969869007

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 80969869007 and manufactured by TECHNOMED EUROPE. 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.

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80969869007
Registration Details
ANVISA Registration Number: 80969869007
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Device Details

KIT ESTIMULADOR EM CLIPE PARA LLIF
Risk Class II

Registration Details

80969869007

25351420130202220

13598814000111

Company Information

TECHNOMED EUROPE
Netherlands
PT: HOLANDA (PAÍSES BAIXOS)

Dates and Status

Nov 07, 2022

VIGENTE

09/18/2025 19:00:01