CE-IVDR IgD assays for Turbidimetry and Nephelometry
TRIMERO Diagnostics is delighted to announce that we have begun to manufacturing our IgD Immunoglobulin assays, in accordance with the requirements of the Regulation (EU) 2017/746 on in vitro diagnostic medical devices, and will therefore be IVDR Certified.
TRIMERO offers IgD assays for:
– Clinical Chemistry Analyzers (turbidimetric method)
– Siemens Healthcare BN™ Series and Atellica® NEPH 630 nephelometers
– Beckman Coulter IMMAGE® 800 Immunochemical Systems
The main features of the assays are:
- turbidimetric method available for most popular clinical chemistry analyzers
- developed specifically for IMMAGE® and BN™ nephelometers
- particle-enhanced reagents for good sensitivity
- based on specific polyclonal antibodies
- calibrators based on polyclonal human serum
- values traced to the British Research Standard for IgD (code: 67/037) of the National Institute for Biological Standards and Controls (a WHO Laboratory for Biological Standards)
Other available TRIMERO nephelometric and turbidimetric assays include:
KLoneus® Free Light Chains (FLC) for serum and urine, Serum Amyloid A (SAA), Retinol Binding Protein (RBP) for serum and urine, Soluble Transferrin Receptor (sTfR), Hemopexin, Cystatin-C for serum and urine, A1-Microglobulin, B2-Microglobulin for serum and urine, Kappa and Lambda Light Chains for serum and urine, Complement C1q, Complement C5, Factor B (C3 Proactivator), C1 (Esterase) Inhibitor.
