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ELECTROLYTES - ANVISA Registration 81996070061

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 81996070061 and manufactured by DIAGFAST PRODUTOS PARA LABORATORIOS LTDA. The registration is held by DIAGFAST PRODUTOS PARA LABORATORIOS 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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81996070061
Registration Details
ANVISA Registration Number: 81996070061
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Device Details

Kit ISE DIAG PACK
Risk Class II

Registration Details

81996070061

25351001696202507

30984754000194

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 05, 2025

VIGENTE

09/18/2025 19:00:01