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Vacuum Regulator - ANVISA Registration 10432309020

Access comprehensive regulatory information for Vacuum Regulator in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10432309020 and manufactured by UNITEC INDUSTRIA E COMERCIO DE APARELHOS HOSPITALARES LTDA. The registration is held by UNITEC INDUSTRIA E COMERCIO DE APARELHOS 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 JG MORIYA REPRESENTAÇÃO IMPORTADORA EXPORTADORA COMERCIAL LTDA, Technologie Medicale, 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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10432309020
Registration Details
ANVISA Registration Number: 10432309020
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Device Details

REGULADOR PARA ASPIRAÇÃO
Risk Class II

Registration Details

10432309020

25351054970202532

50328590000154

Company Information

Dates and Status

May 12, 2025

VIGENTE

09/18/2025 19:00:01