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Blood Parameter Monitoring System - ANVISA Registration 80259110099

Access comprehensive regulatory information for Blood Parameter Monitoring System in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80259110099 and manufactured by PULSION MEDICAL SYSTEMS SE. The registration is held by GETINGE DO BRASIL EQUIPAMENTOS MEDICOS LTDA. with validity until Jun 29, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS, LIDCO LTD, 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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80259110099
2 Related Devices
Registration Details
ANVISA Registration Number: 80259110099
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Related Devices (2)

Monitor de Hemodinâmica PulsioFlex PC4000
Risk Class III

Registration Details

80259110099

25351229659201561

06028137000130

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jun 29, 2015

29/06/2035

09/18/2025 19:00:01

Monitor de Hemodinâmica PulsioFlex PC4000
Risk Class III

Registration Details

80259110099

25351229659201561

06028137000130

Company Information

Dates and Status

Jun 29, 2015

29/06/2035

09/18/2025 19:00:01