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♦ NO DEDICATED CITRATE TUBE NEEDED

the test is performed on blood samples collected in the same top lavender tubes used for full blood count

♦ USER FRIENDLY

continuous loading of samples, touch screen interface, USB port and Bluetooth connection to PC, Tablet and Smartphone

♦ ENVIRONMENTALLY FRIENDLY

no production of waste materials, no extra-costs for waste disposal

♦ NO BIOLOGICAL RISK

ESR is determined in the same full cell count closed tube:
No contact with blood;
No blood is withdrawn;
No liquid waste is produced.

Standard application

♦ EN 61326-1 “Electrical Equipment for Measurement, Control, and Laboratory Use – Electromagnetic compatibility requirements-Part 1: General requirements”
♦ EN 61326-2-6 “Electrical Equipment for Measurement, Control, and Laboratory Use – Electromagnetic compatibility requirements-Part 2-6: In Vitro Diagnostic (IVD) medical equipment”
♦ EN 61010-2-081 Safety for electrical equipment for measurement, control, laboratory use – Part 2-081: Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes (CEI 66-8)”.
♦ – EN 61010-2-101 “Safety for electrical equipment for measurement, control, laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment”.
♦ – 2014/35/EC “Low voltage directive”
♦ – 2014/30/EC “Directive on the harmonisation of the laws of the Member States relating to electromagnetic compatibility”
♦ – 2011/65/EU “Directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment – RoHS2”
♦ – UNI EN ISO 18113-3 Information provided by the manufacturer (labeling) – Part 3: in vitro diagnostic instruments for professional use
♦ – UNI EN ISO 22870 Point of care testing (IOCT) – Requirements for quality and competence
♦ – Clinical and Laboratory Standards Institute, H02-A5, Procedures for the Erythrocyte Sedimentation Rate Test; Approved Standard—Fifth Edition