Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume ; 150 microliter
stored at 4-30 DegreeC
Cat No : CFPC-23-1
PCT
Assessing initial risk of bacterial infection and fatal sepsis
Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock.
INTENDED USE :
ichroma PCT is a fluorescence Immunoassay (FIA) for the quantitative determination of Procalcitonin (PCT) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.
The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PCT concentration in sample.
STORAGE AND STABILITY:
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.
MATERIALS SUPPLIED :
REF CFPC-23
Components of ichromaâ?¢ PCT Cartridge Box:
- Cartridges 10
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer tubes
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample : whole blood (AFIAS), plasma, serum
Reaction Time : 15mins
Detection Range : ichroma(TM) (1 - 100 mIU/ml)
Cat No : CEPC-35
Follicle-stimulating Hormone (FSH)
Diagnosis of early menopause & ovarian degeneration and infertility
This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.
Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample Volume : 30 Microliter
Sample : human serum / plasma / control
Reaction Time ; 10 mins
Cat No : CFPC-32
Ferritin
Monitoring deficiency/excess of iron & inflammation
Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Too little ferritin can lead to anemia, while too much to liver disease, rheumatoid arthritis, other inflammatory conditions, or hyperthyroidism. The ferritin test measures the level of ferritin in the blood.
INTENDED USE :
ichromaâ?¢ Ferritin is a fluorescence Immunoassay (FIA) for the quantitative determination of Ferritin in human serum/plasma. It is useful as an aid for quantifying human ferritin.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigen in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by Instrument for ichrom tests to show ferritin concentration in sample.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/control
Specimen volume : 50 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-89
INTENDED USE :
ichroma AMH is a fluorescence Immunoassay (FIA) for the quantitative determination of AMH (Anti-m�¼llerian hormone) in human serum/plasma. It is useful as an aid in management and monitoring of premature ovarian insufficiency, menopause and ovarian reserve.For in vitro diagnostic use only.
COMPONENTS :
ichroma AMH consists of cartridges, detectors and diluent The cartridge contains the membrane called a test strip which has streptavidin at the test line and chicken IgY at the control line. All cartridges are individually sealed in an aluminum foil pouch containing a desiccant in a box The detector has 2 granules containing anti human AMH-fluorescence conjugate, anti-chicken IgY-fluorescence conjugate, anti-human AMH-biotin conjugate, bovine serum albumin (BSA) and sucrose as a stabilizer, MAB33 as a blocker in Tris-HCl buffer. All detectors are packed in a box The diluent contains bovine serum albumin and NaCl as a stabilizer, tween 20 and CA-630 as a surfactant and sodium azide as a preservative in phosphate buffered saline (PBS), and it is pre-dispensed in a vial. The diluent is packed in a box.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.More antigens in sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show human AMH concentration in the sample.
INTERPRETATION OF TEST RESULT :
The instrument for ichroma tests calculates the test result automatically and displays AMH concentration of the test sample in terms of ng/mL The working range: 0.02- 15 ng/mL
Product Details:
Model Name/Number : FS-114
Brand : Wondfo
Temperature Control : Provide better reaction condition
Convenient : easy to carry
Portable : Small in size 7800mAh built-in battery
Finecare FIA Meter Plus SEThe analyzer is intended for use by healthcare professionals to improve the way to diagnosing and monitoring various conditions, including COVID-19, diabetes, renal injury, cardiovascular disease, pregnancy, inflammation, tumor, etc
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Number of Reactions(Preps)/Kit : 30T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0101C
Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 �¼mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 �¼mol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
Shelf life: 24 month
Individually sealed foil pouches containing:
One cassette device
One desiccant
5L capillary tubes
Sample diluent (REF SB-R0101, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 Test
Samples : Serum/Plasma
Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin
Storage Temperature : 4 - 30 DegreeC
Cat No : CFPC-21
Progesterone
Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy
The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy.
PRINCIPLE :
The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : whole blood/serum/plasma
Sample volume : 75 Microliter
stored at 4 - 30 DegreeC
Cat No i CHROMA PSA-25
Prostate Specific Antigen (PSA)
Screening for the prostate cancer & monitoring the effects of the treatment
This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 Test
Samples : Whole blood
Sample volume : 75 Microliter
Cat No : CFPC-38
Storage Temperature ; 4 - 30 DegreeC
HbA1c
Assessing the level of glycated hemoglobin in the blood
This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months.
INTENDED USE
ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. For in vitro diagnostic use only.
PRINCIPLE:
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human serum/plasma
Specimen volume : 150 Microliter
stored at 4 - 30 DegreeC.
Cat. No : CFPC-22
Thyroid Stimulating Hormone (TSH)
Diagnosing thyroid dysfunction
One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH).
INTENDED USE :
ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip.
More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample.
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 T
Samples: human whole blood/serum /plasma
Specimen volume human whole blood/serum/ plasma
stored at 4-30 C
Cat. No. : CFPC-66
Human Chorionic Gonadotropin (�²-hCG)
Distinguish pregnancy and abnormal pregnancy
The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome.
INTENDED USE :
ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the
quantitative determination of -HCG in human whole blood/serum
/plasma. It is useful as an aid in management and monitoring of beta
human chorionic gonadotropin (hCG) level in human
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; Dried
antibodies in the detector tube, once diluted with the diluent, bind
with antigens in the sample to form antigen-antibody complexes.
These complexes then migrate through the nitrocellulose matrix and
are captured by another sets of immobilized antibodies on the test line.
The more antigens in the sample, the more antigen-antibody
complexes, which leads to a stronger fluorescence signal. This signal
then is interpreted by the reader to display the �²-HCG concentration in
the sample.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in the original
aluminum foil pouch) if stored at 4-30 C.
The detector, diluent and sample diluent are stable for 20 months
if stored at 2-8 C.
After the cartridge pouch is opened, the test should be
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Specimen : Human serum/plasma/ control
Specimen volume : 75 microliter
stored at 4 - 30 DegreeC.
Cat No : CFPC-26
T4
Assessing to diagnosis & to monitor thyroid diseases(T4)
Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid.
INTENDED USE :
ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human serum/plasma/ control
Specimen volume : 75 Microliter
stored at ; 4 - 30 DegreeC
Cat No ; CFPC-44
T3
Assessing to diagnosis & to monitor thyroid diseases(T3)
This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement.
INTENDED USE :
ichroma T3 is a fluorescence Immunoassay (FIA) for the
quantitative determination of triiodothyronine (total T3) in
human serum/plasma. It is useful as an aid in management
and monitoring of determination of thyroid disorders.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method.
In this method, the analyte in the sample binds to the
fluorescence labeled (FL) detection antibody in detection
buffer, to form the complex as sample mixture. This complex
is loaded to migrate onto the nitrocellulose matrix, where
the covalent couple of T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated,
resulting in less fluorescence signal.
Cat No :14FK10 Bioline* Rotavirus test is an immunochromatographic assay for the detection of Group A rotavirus in human fecal specimens. The test utilizes two kinds of antibody in a solid phase sandwitch immunochromatography to detect group specific proteins, including the major inner capsid protein, present in Group A rotaviruses.
â?¢ Early detection of rotavirus antigen group A all serotype
Shelf life and storage temperature: 18 months from the date of manufacturing at1-30 C
Performance: Sensitivity: 94 %, Specificity 98.3 % (vs. RT-PCR)
Cat No : 11FK50. Bioline DENGUE NS1 Ag TEST FOR EARLY CLINICAL PHASE OF DENGUE INFECTION
Bioline Dengue NS1 Ag rapid test is an in vitro immunochromatographic assay designed to detect Dengue virus NS1 antigen in human serum, plasma or whole blood.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Benefits:
Diagnosis of early acute dengue infection by detecting dengue NS1 antigen
Dengue NS1 antigen can be detected from 1 day after onset of fever
Specimen : Serum, plasma or whole blood (100�¼l)
Test result : 15~20 minutes
Specification:
Sensitivity 92.4%, Specificity 98.4%
CAT No : PI19FRC25. First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40C.
Specimen Type- Whole Blood.
Cat No : PI19FRC25. First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
100% - Specificity
100% - Sensitivity
Detects antibodies specific to Treponema pallidum
Rapid Result time within 20-25 Minutes
Storage at 4-30C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
CAT No : RK026-30. STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CAT No : RK025-40. One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood
Kit Contents:
Standard Q Malaria Pf/PV Ag cassette x 40
Specimen transfer device 3 microlitre x 40
Butter bottle 3m1 x 02
Instructions for use x 01
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and CAT Cat.No : RK025-40. Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity
Advantage:
Distinguish the infection between P.falciparum and P.vivax
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5�µl)
Room temperature storage.
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