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ELECTROLYTES - ANVISA Registration 80312130009

Access comprehensive regulatory information for ELECTROLYTES in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80312130009 and manufactured by DIAMOND DIAGNOSTICS, INC. The registration is held by MONZON COMÉRCIO DE PRODUTOS LABORATORIAIS E 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 CARETIUM MEDICAL INSTRUMENTS CO.,LIMITED, ROCHE DIAGNOSTICS GMBH, 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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80312130009
Registration Details
ANVISA Registration Number: 80312130009
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Device Details

ISE Fluid Pack
Risk Class II

Registration Details

80312130009

25351030107201507

07534785000121

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 30, 2015

VIGENTE

09/18/2025 19:00:01