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AMMONIA - ANVISA Registration 81246980004

Access comprehensive regulatory information for AMMONIA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81246980004 and manufactured by ORTHO CLINICAL DIAGNOSTIC, INC. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE 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 ROCHE DIAGNOSTICS GMBH, SIEMENS HEALTHCARE DIAGNOSTICS INC., 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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81246980004
Registration Details
ANVISA Registration Number: 81246980004
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Device Details

REATIVO SECO VITROS PARA AMONIA AMON/NH3
Risk Class II

Registration Details

81246980004

25351455192201795

21921393000146

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2017

VIGENTE

09/18/2025 19:00:01