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Pressure and Volume Ventilator - ANVISA Registration 82776280002

Access comprehensive regulatory information for Pressure and Volume Ventilator in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82776280002 and manufactured by Pró-Life Equipamentos médicos ltda. The registration is held by Pró-Life Equipamentos médicos ltda with validity until Sep 16, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD., MAQUET CRITICAL CARE AB, 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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82776280002
Registration Details
ANVISA Registration Number: 82776280002
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Device Details

VentSmart Pro - Ventiladores Pulmonares ProLife
Risk Class III

Registration Details

82776280002

25351384648202454

66783630000430

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 16, 2024

16/09/2034

09/18/2025 19:00:01