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.
Device Details
Registration Details
80146502203
25351133085201971
56998701000116
Company Information
Dates and Status
Jun 03, 2019
VIGENTE
09/18/2025 19:00:01
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBHโข Germany
THE BINDING SITE GROUP LTDโข United Kingdom
DIAZYME LABORATORIES, INC.โข United States of America
BECKMAN COULTER INC.โข United States of America
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH.โข Germany
CADEIA KAPPA/LAMBDA
Famรญlia Lambda Cadeia Leve
KATAL BIOTECNOLOGICA INDรSTRIA E COMรRCIO LTDA
10377390295
Mar 05, 2025
CADEIA KAPPA/LAMBDA
Famรญlia Diazyme Human Kappa Free Light Chain
DIAZYME LABORATORIES, INC.
82444370042
Mar 06, 2023
CADEIA KAPPA/LAMBDA
Famรญlia Diazyme Human Lambda Free Light Chain
DIAZYME LABORATORIES, INC.
82444370043
Mar 06, 2023
CADEIA KAPPA/LAMBDA
LAMB2 (Tina-quant Lambda Gen.2)
ROCHE DIAGNOSTICS GMBH
10287411495
Jun 15, 2020
CADEIA KAPPA/LAMBDA
Alinity c Kappa Light Chains Reagent Kit
SENTINEL CH. SPA
80146502255
Jun 15, 2020

