The Haemonetics Cell Saver 5/5+ Bowl Kit with the product code 225M004C is a component of the Haemonetics Cell Saver 5 and Cell Saver 5+ autotransfusion systems. These systems are used in medical settings, particularly during surgeries, to collect, process, and reinfuse a patient's own blood that is lost during the procedure.
Here are some general features and considerations related to the Haemonetics Cell Saver 5/5+ Bowl Kit:
Autotransfusion System: The Haemonetics Cell Saver 5/5+ is an autotransfusion system designed for blood salvage during surgery. It helps minimize the need for allogeneic blood transfusions.
Bowl Kit: The Bowl Kit is a critical component of the system, and it typically includes a collection bowl where blood is collected, processed, and washed before being returned to the patient.
Compatibility: The Bowl Kit is designed to be compatible with the Cell Saver 5 and Cell Saver 5+ devices.
Processing Blood: The autotransfusion system processes shed blood from the surgical field, removes unwanted materials, and returns the washed blood to the patient.
225M004C: The specific product code is used for identification and ordering purposes. It helps in ensuring that the correct component or kit is being used.
One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces)
Cat. No.: RH0301T
INTENDED USE
The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing.
PRINCIPLE
The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary.
STORAGE
The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch.
WARNING AND PRECAUTIONS
1. For in vitro diagnostic use only.
2. Do not use kit beyond the expiration date.
3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures.
4. The test device should not be reused.
REAGENTS AND MATERIALS PROVIDED
1. One pouched cassette with desiccant.
2. One operating Instruction
MATERIALS REQUIRED BUT NOT PROVIDED
1. Clock or Timer
SPECIMEN COLLECTION AND PREPARATION
1. Collect stool sample by using the sample collection device provided.
2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample.
3. Put the sample collection stick back in the sample collection device and screw together tightly.
4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing.
ASSAY PROCEDURE
1. Remove the test device from foil pouch by tearing along the notch.
2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION
3. Shake the sample collection device several times.
4. Holding the sample collection device upright, carefully unscrew the tip of collection device.
5. Squeeze 2-3 drops of the sample solution on the test sample pad.
6. Read the test results in 5 minutes.
INTERPRETATION OF RESULTS
Negative: Only one colored band appears on the control region (C). No colored band in the test region (T).
Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T).
Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.
1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma.
2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.
3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
Test Procedure
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) 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.
3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below.
4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Interpretation of Results
Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is.
Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region.
Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
Product Description : Covid19 test kits
Product origin : Korea
Payment Terms : Pay By 100% T/T in advance
Shipping Terms : after deposit confirm
price: Negotiable
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The kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Human
Androgen in samples. Add Androgen to monoclonal antibody Enzyme well which is pre-coated with Human
Androgenmonoclonal antibody, incubation; then, add Androgenantibodies labeled with biotin, and combined with
Streptavidin-HRP to form immune complex; then carry out incubation and washing again to remove the uncombined enzyme.
Then add Chromogen Solution A, B, the color of the liquid changes into the blue, And at the effect of acid, the color finally
becomes yellow. The chroma of color and the concentration of the Human Substance Androgen of sample were positively
correlated.
