AMMONIA - ANVISA Registration 80146502238

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 80146502238 and manufactured by SENTINEL CH. SPA. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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80146502238
Registration Details
ANVISA Registration Number: 80146502238
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Família Alinity c Ammonia Ultra
Risk Class II

Registration Details

80146502238

25351576741201926

56998701000116

Company Information

SENTINEL CH. SPA
Italy
PT: ITÁLIA

Dates and Status

Dec 16, 2019

VIGENTE

09/18/2025 19:00:01