Platelet aggregation assay system; Hematracer Zen

Platelet aggregation assay system; Hematracer Zen

 For monitoring of antiplatelet drugs! (Aspirin, Clopidogrel, etc.)
 Whole blood can be tested as is (no need for centrifugation)
 Sample volume 0.8mℓ/1test
 No influence of chyle or blood cell contamination
 Compact size includes in the touch panel and printer
 Easy maintenance

Specifications

Product Description The platelet aggregation is a test to check the aggregation ability (hemostatic ability) of platelets. If the platelet aggregation ability is too strong, clots tend to form and it is necessary to be careful of thrombotic diseases such as myocardial infarction and cerebral infarction. If the platelet aggregation ability is too strong, a thrombus can easily form, and it is necessary to be careful about thrombotic diseases such as myocardial infarction and cerebral infarction. If the platelet aggregation ability is too strong, a thrombus can easily form, and you need to be careful about thrombotic diseases such as myocardial infarction and cerebral infarction. On the other hand, if the aggregation ability is too weak, caution is needed in case of bleeding. Currently, in addition to determining platelet function, this test is also used to check the amount and type of drugs used in antiplatelet therapy (administration of antiplatelet drugs) for the treatment and prevention of cerebral infarction and myocardial infarction.
Specifications Principle:   SFP variation method (narrow mouth suction pressure detection method)
Filter size: 30μm x 30μm, 300 ports / 1.0 mm diameter
Test items: ADP(Adenosine diphosphate), collagen, etc.
Samples: Whole blood or PRP (platelet rich plasma) with anticoagulant sodium citrate)
Required Sample Volume: Approx. 1 ml for one test
Measurement time: Approx. 7 minutes
Build-in:      Touch panel and printer, USB, RS232C
Options: Reagent cooler and Barcode reader
Dimensions: 315(W)×360(D)×340(H)mm
Weight: 13.5kg
Power supply: AC100V 50/60Hz, Power consumption: 65VA

Medical device registration number 13B3X00181000004
Class classification General medical device (Class I)
Compliant with IEC61010-1(JIS C 1010-1) , IEC61326-2-6