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Vacuum Regulator - ANVISA Registration 80204410033

Access comprehensive regulatory information for Vacuum Regulator in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80204410033 and manufactured by AIR LIQUIDE MEDICAL SYSTEMS S.A.. The registration is held by AIR LIQUIDE BRASIL 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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80204410033
Registration Details
ANVISA Registration Number: 80204410033
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Device Details

REGULADOR DE VÁCUO ALIZE
Risk Class I

Registration Details

80204410033

25351185505201746

00331788000119

Company Information

France
PT: FRANÇA

Dates and Status

Jul 17, 2017

VIGENTE

09/18/2025 19:00:01