Company - AESKU.GROUP - Experts in Diagnostics

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News

March 2019

AESQC IFA Products Receive CE Marking, FDA Registration

AESKU announces completion of CE Marking and FDA registration for new ICAP compatible AESQC IFA quality control products for use with Immunofluorescence Assays (IFA), including clinical anti-nuclear antibody (ANA) testing.
Worldwide

09/10/2019

14th Dresden Symposium on Autoantibodies, Dresden Fair, Booth 6

Visit AESKU at the 14th Dresden Symposium on Autoantibodies (DSA) - From September 10th to 13, 2019.
Dresden Germany

March 2018

nDNA (Crithidia luciliae) now FDA cleared with HELIOS System

AESKU Receives FDA 510(k) Clearance for nDNA (Crithidia luciliae) with the HELIOS AUTOMATED IFA SYSTEM.
USA

04/03/2018

ICAP Compatible IFA Quality Controls Now Available from AESKU

AESKU announces a new ICAP compatible Immunofluorescence Assay (IFA) Quality Control (QC) product line and supporting Quality Assurance tool, AESQC.com, to help laboratories identify, correct, and prevent analytical failure prior to releasing results.
Worldwide

April 2018

FDA clears Automated Vasculitis Test from AESKU

AESKU Receives FDA 510(k) Clearance for Anti-Neutrophil Cytoplasmic Antibody (ANCA) test to aid in the Diagnosis of ANCA Associated Vasculitides with the HELIOS Automated immunofluorescence assay (IFA) System
USA