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KAPPA/LAMBDA CHAIN - ANVISA Registration 80146502203

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 80146502203 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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80146502203
Registration Details
ANVISA Registration Number: 80146502203
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Device Details

Alinity c Lambda Light Chains Reagent Kit
Risk Class II

Registration Details

80146502203

25351133085201971

56998701000116

Company Information

SENTINEL CH SPA
Italy
PT: ITรLIA

Dates and Status

Jun 03, 2019

VIGENTE

09/18/2025 19:00:01