IVD

Multichem^® U – Urinary Chemistry QC

Multichem U Control, from Technopath Manufacturing Ltd, is intended for use as a third party, bi- level, liquid stable, multi-analyte control designed for use in the routine monitoring of precision of laboratory testing procedures. Target values are provided for 13 analytes including kidney function parameters, pituitary/adrenal metabolites, hCG and urinary proteins. Multichem U Control is designed as a bi-level liquid stable product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at 2°C to 8°C and mixed as per IFU prior to use. The control is to be stored at 2 to 8°C between use.

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Multichem^® WBT – Whole Blood Immunosuppressant QC

Multichem WBT Control, from Technopath Manufacturing Ltd, is intended for use as a third-party, tri- level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Cyclosporine, Tacrolimus and Sirolimus Assays. Multichem WBT Control is designed as a tri-level, liquid stable frozen product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.

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PK Range – Extended Phenotyping

Extended phenotyping reagents for BECKMAN COULTER PK7300 & PK7400 Automated Microplate Systems The reagents of PK7300 are in vitro diagnostic medical devices (IVDMD) for professional use. They are exclusively intended for blood bag identification centres, such as blood banks. The reagents ANTI-Fya (FY1) PK, ANTI-Fyb (FY2) PK, ANTI-Jka (JK1) PK, ANTI-Jkb (JK2) PK, ANTI-M (MNS1) PK, ANTI-N (MNS2) PK, ANTI-S (MNS3) PK and ANTI-s (MNS4) PK are used for the extended phenotyping of human red blood cells. They detect the presence of antigens Fya (FY1), Fyb (FY2), Jka (JK1), Jkb (JK2), M (MNS1), N (MNS2), S (MNS3) and s (MNS4) on the surface of red blood cells. The CONTROL PK must be used in blood grouping or phenotyping. It is devoid of antibody activity. When tested under the same conditions as the reagents for PK®SYSTEM, the CONTROL PK enables the user to interpret the result obtained. These reagents are ready for use for BECKMAN COULTER PK7300 & PK7400 automated microplate systems.

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QWALYS^® 3 EVO

Innovation and flexibility for your immunohaematology automation DIAGAST, an international expert and specialist in transfusion diagnostics, has included innovation and flexibility in the QWALYS^® 3 EVO automated system. With the E.M.® Technology, QWALYS^® 3 EVO is the only fully-automated system on the market using the magnetisation of erythrocytes, a process that no longer requires washing and centrifugation steps. Latest-generation and fully-automated system with high throughput, large loading capacity and STAT function among others, QWALYS^® 3 EVO is the benchmark instrument for all laboratories, blood banks, blood transfusion centres and hospitals.

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Safety Test ABO
Confirm ABO Blood Group at patient bedside Safety Test ABO is a medical in vitro diagnostic device for professional use to confirm ABO blood group compatibility before a transfusion, at the patient's bedside. This testing comes in addition to patient identity checking and comparison between group on blood bag label and the patient’s group. The procedure is based on haemagglutination’s principles. Red blood cells carry antigens and agglutinate in the presence of test sera (reagents) carrying corresponding antibodies (colored reagents are dried out on the card’s wells). Safety Test ABO (Ref 79069) includes 100 single-use tests packed separately. A single test of Safety Test ABO consists of:

1 Safety Card AB is individually packed in a sealed package 1 vial of NaCl 0,9% (physiological saline) 1 fingerprick lancet 1 segment opener 4 spatulas

Safety Card AB Safety Card AB (Ref 79074) contains 100 cards for single use, and each card is individually packed in a sealed package. This package contains as well a transparent adhesive sheet and a technical insert. Safety Card AB contains 4 spots with dried reagents:

1 x anti-A and 1 x anti-B for the patient on the card’s left side 1 x anti-A and 1 x anti-B for the blood bag on the card’s right side
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Serum Indices Quality Control

Your perfect tool to aid in the monitoring of instrument detection of Haemolysis, Icterus and Lipaemia in specimens. Fortress Serum Indices Quality Control are designed to monitor the ability of an instrument to accurately measure HIL in specimens. This is done through the manufacture of control material which mimics specimens that would be considered normal, haemolytic, icteric, and lipaemic using human based products. Ensure accurate monitoring of patient samples for Serum Indices by running this QC daily.

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Urinalysis
Urinalysis Systems from Mindray Urinalysis remains one of the most widely performed diagnostic tests in the clinical laboratory, supporting early detection and monitoring of kidney disease, urinary tract infections (UTIs), metabolic disorders, and systemic conditions. Technopath is proud to supply the Mindray Urinalysis portfolio—a comprehensive range of automated urine chemistry analysers, urine sediment systems, and fully integrated urinalysis automation lines designed to improve diagnostic accuracy, standardisation, and laboratory efficiency. Why Choose Technopath for Urinalysis Solutions?
Trusted distribution partner for Mindray in Ireland & the UK
Application and technical support tailored to clinical laboratories
Expertise across IVD, pathology, and laboratory diagnostics
Support for laboratory accreditation and quality standards (e.g. ISO 15189)
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VALIDATE^® ACTH
ACTH Chemistry Linearity Verification and Calibration Kits Adrenocorticotropic Hormone analyte for your Roche cobas^® clinical analyser.
CE Marked
Adrenocorticotropic Hormone Analyte Available
Human Plasma Matrix
Liquid, Ready-to-Use
Analyte Summary by available Product ACTH: ACTH
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VALIDATE^® Anaemia
Anaemia Linearity Verification and Calibration Kits View the multiple range coverages for each analyte and identify the recommended products for your specific clinical analyser.
CE Marked
3 Analytes Available
Ferritin, Folate, Vitamin B12
Human Serum Matrix
Liquid, Ready-to-Use
Analyte Summary by Anaemia Product ANEMIA: B12, FERR, FOL FERRITIN: FERR
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VALIDATE^® Body Fluids
Body Fluids Linearity Verification and Calibration Kits Body Fluids Linearity Verification and Calibration Kits for your Roche cobas^® clinical analyser.
CE Marked
19 Analytes Available
Liquid, Ready-to-Use
Analyte Summary by available Product BF: ALB,AMY,CA 19-9,CEA,CHOL,CREA,GLU,LAC,LD,TP,TRIG,UN,CSF-TP BF2: ALP,CA,CL,K,NA,TB,UA
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VALIDATE^® Bone
Bone Linearity Verification and Calibration Kits View the multiple range coverages for each analyte and identify the recommended products for your specific clinical analyser.
CE Marked
2 Analytes Available
Parathyroid Hormone, Vitamin D
Liquid, Ready-to-Use
Available Bone Products and Analyte Summary PTH: Parathyroid Hormone VIT D: Vitamin D
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VALIDATE^® Cardiac
Cardiac Linearity Verification and Calibration Kits View the multiple range coverages for each analyte and identify the recommended products for your specific clinical analyser.
CE Marked
12 Analytes Available
Human Serum Matrix
Liquid, Ready-to-Use
Analyte Summary by Cardiac Product CM1: CK-MB,MYO CM2:BNP,hs-CRP,NT-proBNP,TnI,TnT,NT-proBNP (CR) CM32:HCY,LP(a) hsTROPONIN:hsTNT, hsTNI
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