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FRUCTOSAMINE - ANVISA Registration 10033121019

Access comprehensive regulatory information for FRUCTOSAMINE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10033121019 and manufactured by SENTINEL CH. SPA. The registration is held by BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO 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 HORIBA ABX SAS, 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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10033121019
Registration Details
ANVISA Registration Number: 10033121019
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Device Details

Família de Reagente, Calibrador e Controle Fructosamine Sentinel
Risk Class II

Registration Details

10033121019

25351503713202112

42160812000144

Company Information

SENTINEL CH. SPA
Italy
PT: ITÁLIA

Dates and Status

May 27, 2021

VIGENTE

09/18/2025 19:00:01