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Plethysmograph - ANVISA Registration 80102512071

Access comprehensive regulatory information for Plethysmograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102512071 and manufactured by VYAIRE MEDICAL GMBH. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS Mร‰DICOS 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 TIMPEL S.A., EKOVUK MEDI S.R.O., 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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80102512071
Registration Details
ANVISA Registration Number: 80102512071
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Device Details

DISPOSITIVO DE FUNร‡รƒO PULMONAR
Risk Class II

Registration Details

80102512071

25351284832201857

04718143000194

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jul 09, 2018

VIGENTE

09/18/2025 19:00:01