Disposable Cesarean Drape With Fluid Collection Pouch
Product Details:
Minimum Order Quantity 10 Piece
Type Incise drapes
Material Non Woven
Usage/Application Hospital
Gender Unisex
Is It Waterproof Waterproof
Absorbency Yes
Fluid Repellent Yes
Fluid Impervious No
Manufactured By Om Sai Enterprises
Sterility Sterile
Country of Origin Made in India
These DISPOSABLE CESAREAN Drapes are the best option for all kinds of surgeries. We always use the high-grade raw material to manufacture these disposable drapes. We provide 10 pcs in single packing as per your request. We are providing the best quality and standard size product that provides comfort in hospital rooms. we provide various color options in this disposable drape and the product can be customized as the client requirements.
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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.
One Step Troponin Test (Whole blood/Serum/Plasma
FOR IN VITRO DIAGNOSTIC USE ONLY
SPECIMEN COLLECTION
1. Testing should be performed immediately after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods. Specimens may be stored at 2-8C for up to 3 days. For long-term storage, specimens should be kept below -20C.
2. 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.
MATERIALS PROVIDED
1. Test cards individually foil pouched with a desiccant
2. Plastic dropper
3. Package insert
MATERIALS REQUIRED BUT NOT PROVIDED
1. Timer/clock
2. Pipette
3. Controls
ASSAY PROCEDURE
1. Read package insert carefully before testing. Allow the test devices, whole blood, serum or plasma to equilibrate to room temperature (15-30C) prior to testing. Do not open pouches until ready to perform the assay.
2. Remove the test device from the foil pouch and use it as soon as possible.
3. Place the test device on a clean and level surface. Hold the dropper provided vertically and transfer 3 drops of specimen (100�µl) to the specimen well (S) in the test device.
4. Wait for the red line(s) to appear. The result should be read between 10 to 15 minutes.
INTERPRETATION OF RESULTS
1. Positive Two colored lines should be observed in the viewing window. The line in the test region (T) is the probe line; the line in the control region (C) is the control line, which is used to indicate proper performance of the device. The color intensity of the test line may be weaker or stronger than that of the control line.
2. Negative The control line appears in the test window, but the test line is not visible.
3. Invalid No line appears in the control region. Under no circumstances should a positive sample be identified until the control line forms in the viewing area. If the control line does not form, the test result is inconclusive and the assay should be repeated.
Anti-Syphilis Test is a rapid direct binding test for the visual detection of anti-syphilis antibodies
in serum as an aid in the diagnosis of syphilis infection. Test results are read visually without any
instrument. It is based on the principle of double antigen sandwich immunoassay for determination of syphilis antibodies in serum. Purified recombinant syphilis antigens are employed to identify
anti-Syphilis antibodies specifically. This one step test is very sensitive and only takes about 10 to 20 minutes.
Syphilis Test SPECIMEN COLLECTION
For serum, collect blood into a container without anticoagulant. Allow the blood to clot and separate the serum from the clot. Use the serum for testing. If the specimen cannot be tested on the day of collection, store the serum specimen in a refrigerator or freezer. Bring the specimens to room temperature before testing. Do not freeze and thaw the specimen repeatedly.
Syphilis Test PROCEDURE
Strip
1.When you are ready to begin testing, open the sealed pouch by tearing along the notch. Remove the test from the pouch.
2. Immerse the strip into the container with the arrow end pointing towards the container. Do not immerse past the MAX (maximum) line.
Take the strip out after 8-10 seconds and lay the strip flat on a clean, dry, onabsorbent surface (e.g., mouth of the serum container).
3.Wait 10-15 minutes and read result. Do not read results after 20 minutes.
Cassette
1. Open a pouch containing a cassette, lay the cassette.
2. Using the plastic pipettor provided, draw about 2-3 drops (100mL) the sample into the sample well of the cassette.
3. Read results within 10-15 minutes. Do not read results after 20 minutes.
INTERPRETATION OF RESULTS
Negative: Only one pink band appears on test region of the Cassette. This indicates that there is no detectable Anti-Syphilis in the serum.
Positive: Two pink bands appear on test region of the Cassette. This indicates that the specimen contains detectable amount of Anti-Syphilis.
Invalid: If without colored band appears on test region, this is an indication of a possible error in performing the test. The test should be repeated using a new device.
Syphilis Test PRECAUTION:
1. Must use fresh specimen and avoid repetitive freezing, the result will be invalid
2. Use it before expiry date.
3.The package of kit should not be opened until it reaches the room temperature if it taken out from the refrigerator.
4 .Old Serum can not be used. If the serum is thick, it can be used only after being separated.
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.
One Step H. Pylori Ab wb /serum/plasma test is a rapid test for the qualitative detection of antibodies specific to Helicobacter pylori in human serum/plasma and whole blood. In this test kit, the H. pylori antigen â?? colloid gold conjugate and specimen moves along the membrane chromatographically to the test region and forms a visible line as the antigenantibodyantigen gold particle complex forms with high degree of sensitivity and specificity. This one step test only takes about 1015 minutes. Test results are read visually without any instrumentation.
SPECIMEN COLLECTION & PREPARATION
Both whole blood (with or without anticoagulant), serum and plasma specimens can be used with this assay. Simply follow the standard clinical produres to collect whole blood, serum or plasma specimens. If the specimen cannot be tested on the day of collection, store the serum/plasma specimen in a temperature of 28 ºC for up to 72 hours. Stir and bring the specimens to room temperature before testing. Do not freeze whole blood specimens. Do not freeze and thaw the specimen repeatedly. Attention: Specimens and all materials coming in contact with them should be handling and disposed of as if capable of transmitting infection. Avoid contact with skin by wearing gloves and proper laboratory attire.
Connecting Tube with Yankaur Handle
Product Code: MED 109
Specifications: Sterile, individually packed in peelable pouch pack
Size/Strength: Adult, Neo
Description
Rigid, angled, one-piece design, made from clear, medical grade PVC.
Edges are smooth and clean. It has a bulbous tip and ribbed at proximal end
to provide perfect grip.
Clear tips permit visual monitoring of suction fluids.
Connecting tubing with optimal draping qualities for maintaining a wall
thickness to resist the most rugged environments.
Used to clear copious and thick secretions and vomitus from oro-pharyngeal cavity and suction fluids and blood to provide clear surgical field.
