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KAPPA/LAMBDA CHAIN - ANVISA Registration 80146502255

Access comprehensive regulatory information for KAPPA/LAMBDA CHAIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80146502255 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 companies making the same product including SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH, THE BINDING SITE GROUP LTD, 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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80146502255
Registration Details
ANVISA Registration Number: 80146502255
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Device Details

Alinity c Kappa Light Chains Reagent Kit
Risk Class II

Registration Details

80146502255

25351711627201959

56998701000116

Company Information

SENTINEL CH. SPA
Italy
PT: ITรLIA

Dates and Status

Jun 15, 2020

VIGENTE

09/18/2025 19:00:01