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Monitoring Kit - ANVISA Registration 81086970021

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 81086970021 and manufactured by Inomed Medizintechnik GmbH. The registration is held by rbtg brasil equipamentos médicos hospitalares 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 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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81086970021
Registration Details
ANVISA Registration Number: 81086970021
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Device Details

Sonda e Cateter PIOM SDN
Risk Class II

Registration Details

81086970021

25351611717201789

18949207000172

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jan 29, 2018

VIGENTE

09/18/2025 19:00:01