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SARS-COV-2/Influenza A+B Antigen Combo Rapid Test Device
PRODUCT SPECIFICATIONBrandFunworldCertificateCESpecimenNasopharyngeal swabs/ Nasal swabPack20TReading Time10 minutesContentsCassette , Buffer ,Package insertStorage2-30℃Shelf Life2 yearsINTERPRETATION OF RESULTSSame test procedure As SARS-COV-2 Antigen Rapid Test Device (Swab), The result Should be read at 10 minutes, Do not interpret the result after 20 minutes.Possible Interpretation of Test Res -
CRP Rapid Test Device (Whole Blood/Serum/Plasma)
Product Parameters Product NameD-Dimer Rapid Test Strip Used forFor professional in vitro diagnostic use only.SpecimenWhole Blood/Serum/PlasmaMaterials Provided . Individually pouched test strips. Disposable pipettes.Package insert. BufferPacking25 tests/box , 1 test/polybagMOQ1000 testsDiverse Coopetation ModesOEM/ODMPRINCIPLE The D‐Dimer Rapid Test Strip (Whole blood/serum/Plasma) detects D‐Dime -
CRP C-Reactive Protein Semi-Quantitative Rapid Test Strip (WB/S/P) (10~30~60 mg/L)
INTRODUCTION C‐reactive Protein (CrP) in patient’s sera has been found in association with acute infections,necrotic conditions and a variety of inflammatory disorders. There is a strong correlation betweenserum levels of CrP and the onset of the inflammatory process. Monitoring the levels of CrP inpatient’s sera indicates the effectiveness of treatment and the assessment of patient recovery. It i -
iGFBP-1 Rapid Test Device / Strip
PRINCIPLEThe iGFBP‐1 (vaginal secretion) has been designed to detect iGFBP‐1 thrisough visualinterpretation of color development in the internal strip. The membrane was immobilized withanti‐iGFBP‐1 antibodies on the test region. During the test, the specimen is allowed to react withcolored anti‐iGFBP‐1 antibodies colloidal gold conjugates, which were precoated on the samplepad of the test. The mix -
LH One Step Ovulation Test Strip/Device (Urine)
SUMMARY Ovulation is the release of an egg from the ovary. The egg then passes into the fallopian tube where it is ready to be fertilized. In order for pregnancy to occur, the egg must be fertilized by sperm within 24 hours after its release. Immediately prior to ovulation, the body produces a large amount of luteinizing hormone (LH) which triggers the release of a ripened egg from the ovary. This -
hCG One Step Pregnancy Combo Test Device
PRECAUTIONSPlease read all the information in this package insert before performing the test.Do not use after the expiration date printed on the foil pouch.Store in a dry place at 2-30°C or 36-86°F. Do not freeze.Do not use if pouch is torn or damaged.Keep out of the reach of children.For in vitro diagnostic use. Not to be taken internally.Do not open the test foil pouch until you are ready to sta -
Serum Amyloid A Semi-QuantitativeRapid Test Device (Whole Blood/Serum/Plasma)
SUMMARYThe Serum amyloid A (SAA) is normally found complexed with lipoproteins anddifferent isoforms have been described with numbers varying by species.47 SAArepresents one of the most conserved proteins among mammals supporting thepremise that it has a basic and essential role in the innate immune system. Inspecies with CRP, SAA often mirrors the magnitude and time course of theresponse.48 Studi -
D-Dimer Rapid Test Device(Whole Blood/ Plasma)
Product ParametersProduct NameD-Dimer Rapid Test DeviceUsed forFor professional in vitro diagnostic use only.SpecimenWhole Blood/PlasmaMaterials Provided . Individually packed test devices. Disposable pipettes .Package insert. buffer in the dilute tubesPacking25 tests/box , 1 test/polybagMOQ1000 testsDiverse Coopetation ModesOEM/ODMSUMMARYDuring blood coagulation process, fibrinogen is converted t -
Myoglobin/CK-MB/Troponin I Rapid Combo Test Device (WB/S/P)
PRINCIPLEThe Myoglobin/CK‐MB/Troponin I Rapid Combo TestDevice (WholeBlood/Serum/ Plasma)is a qualitative, membrane basedimmunoassayfor the detection of Myoglobin,CK‐MB and TroponinI in wholeblood, serumor plasma.Themembrane is pre‐coated with specific capture antibodies in each of the testlineregions of thetest.During testing,the whole blood,serum or plasma specimen reacts with the particlecoated -
H-FABP Rapid Test Device (Whole Blood/Serum/Plasma)
SPECIMEN COLLECTION AND STORAGE.The h‐FABP Rapid Test Device (Whole Blood/Serum/Plasma) is intended only for use with human whole blood, serum, or plasma specimens..Only clear, non‐hemolyzed specimens are recommended for use with this test. Serum or plasma should beseparated with soonest possible opportunity to avoid hemolysis..Perform the testing immediately after the specimen collection. Do not -
Troponin I Rapid Test Device(Whole Blood/Serum/Plasma)
DIRECTIONS FOR USEAllow test device, specimen, buffer and/or controls to reach room temperature (15‐30°C) prior to testing.1.Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.2.Place the test device on a clean and level surface.For Whole Blood, Serum or Plasma specimens:Hold the dropper vertically and transfer 2 drops -
Troponin I Rapid Test Device (Serum/Plasma)
KIT COMPONENTS.Individually packed test devices.Disposable pipettes.Buffer.Package insertEach device contains a strip with colored conjugates and reactive reagents pre‐spreaded at the corresponding regions，For adding specimens use ，Phosphate buffered saline and preservative For operation instruction.DIRECTIONS FOR USE Allow test device, specimen, buffer and/or controls to reach room temperature (1
