Uncut sheet for Procalcitonin/Interleukin- 6 Rapid Test

short description:

Uncut sheet for  ProcalcitoninInterleukin- 6 Rapid Test
Methodology :Fluorescence Immunochromatographic Assay


  • Testing time: 10-15 minutes
  • Valid Time: 24 month
  • Accurancy: More than 99%
  • Specification: 1/25 test/box
  • Storage temperature : 2℃-30℃
  • Methodology: Fluorescence Immunochromatographic Assay
  • Response timr: 10-15 mins
  • Product Detail

    Product Tags

    PRODUCTION INFORMATION

    Model Number Uncut Sheet for PCT/IL6 Packing 25Tests/ kit, 30kits/CTN
    Name  Uncut sheet for Procalcitonin/Interleukin

     
    Instrument  classification Class II
    Features High sensitivity, Easy opeation Certificate CE/ ISO13485
    Accuracy > 99% Shelf life Two Years
    Methodology FIA  Response Time  10-15 mins
    4

    Superiority

    The kit is high accurate,fast and can be transported at room temperature.It's easy to operate.
    Specimen type : Serum/Plasma/ Whole blood

    Testing time:15 -20mins

    Storage:2-30℃/36-86℉

    Methodology:Fluorescence

     Applicable Instrument :WIZ A101/WIZ A203

     

     

    Feature:

    •  High sensitive

    •  result reading in 15-20 minutes

    •  Easy operation

    •  High Accuracy 

     

    2

    INTENDED USE

    The PCT/IL-6 Rapid Test Device (the "uncut sheet" format for manufacturing use) is a fluorescence immunochromatographic assay intended for the quantitative determination of procalcitonin (PCT) and interleukin-6 (IL-6) concentrations in human serum, plasma, or whole blood specimens.

    This test is intended for in vitro diagnostic professional use and serves as an aid in the clinical assessment of inflammatory response and infection status, including the early diagnosis of bacterial infections, sepsis, and systemic inflammatory response syndrome (SIRS) .

    The combined detection of PCT and IL-6 enables complementary advantages: IL-6 provides early "alert" of infection, while PCT offers high specificity for bacterial sepsis, supporting full-course management of sepsis and guiding appropriate antibiotic therapy . The test employs a fluorescence   immunochromatographicassay usinga double antibody sandwich format

    The device provides quantitative screening results. Test results are intended for clinical reference only. The test result should be interpreted in conjunction with patient history, clinical presentation, and other laboratory findings. 

    This product is intended for use by trained healthcare professionals or laboratory personnel. This product is for manufacturing use only and is intended for further processing into final device format.

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