Monitoring Kit - ANVISA Registration 80259110153

Access comprehensive regulatory information for Monitoring Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80259110153 and manufactured by PULSION MEDICAL SYSTEMS SE. The registration is held by GETINGE DO BRASIL EQUIPAMENTOS MEDICOS LTDA. with validity until Sep 18, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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80259110153
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Registration Details
ANVISA Registration Number: 80259110153
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Kit de Monitorização PiCCO
Risk Class III

Registration Details

80259110153

25351132593201705

06028137000130

Company Information

Germany
PT: ALEMANHA

Dates and Status

Sep 18, 2017

18/09/2027

09/18/2025 19:00:01

Kit de Monitorização PiCCO
Risk Class III

Registration Details

80259110153

25351132593201705

06028137000130

Company Information

Dates and Status

Sep 18, 2017

18/09/2027

09/18/2025 19:00:01