Mowell Plastic Vaginal Speculum Specifications: Item type feminine hygiene Material: Plastic . Suitable for all Package included: 1pc Size: Medium/Large Description Department of Gynaecology. MOWELL Disposable Use Asepsis Dilator Voyeuristic Speculum Cervical Examination.
One Touch Ultra Strip is a part of One Touch device. When used with One Touch meters, these strips measure the concentration of blood glucose by self-testing for both professional and home use. Salient Features: Automatically draws blood into the test strips in a painless manner Fast, painless testing For quick and accurate results Pack Size: 50 strips & 10 strips Warranty: 6 months Directions For Use: OneTouch Ultra Strips are used with the OneTouch Meter for quantitatively measuring glucose in fresh capillary whole blood These Strips and meter are intended for self testing outside the body (in vitro diagnostic use) by people with diabetes at home and health care professionals in the clinical setting, as an aid to monitor the effectiveness of diabetes control OneTouch Ultra Strips and meter are for use on the finger, palm, and forearm Safety Information: Each strip intended for single one time use Keep out of the reach and sight of the children Dispose the used strips properly Store in a cool and dry place
The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip. The system is intended to be used by a single patient and should not be shared. The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended for self-testing outside the body (in vitro diagnostic use) by people with diabetes at home and with their healthcare professionals in a clinical setting as an aid to monitor the effectiveness of diabetes control. The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is not to be used for the diagnosis of or screening of diabetes or for neonatal use. The system is intended to be used by a single patient and should not be shared. Test Principle Glucose in the blood sample mixes with the enzyme Glucose Oxidase (see page 130) in the test strip and a small electric current is produced. The strength of this current changes with the amount of glucose in the blood sample. Your meter measures the current, calculates your blood glucose level, displays the blood glucose result, and stores it in its memory. Use only OneTouch® Selectâ?¢ Plus Control Solutions and Test Strips with the OneTouch® Selectâ?¢ Plus Meter.
OneTouch select plus 50 strips. Select plus siple glucometer strips. New OneTouch select plus simple. So simple, it's advanced Uses It helps to monitor the blood glucose level with comfort at home and helps in keeping diabetes and related issues in check. Salient Features: -Provides accurate and reliable results -Can be measured indoors and outdoors as well -Used for the accurate quantitative measurement of glucose (sugar) present in the blood -The high-low alarm helps in giving the accurate information about one's blood glucose levels -Each strip is meant to be used one-time use -The device includes a lancing device, 10 strip lancets, owners guide, 1 case and 1 High--Low Alarm Reference Card Directions For Use Insert the strip to start and apply blood Reading will appear on the screen Safety Information: - Read the label carefully before use - Keep out of the reach of children - Do not refrigerate -Store in a cool dry place -Do not use if the expiry date has passed -To be used within 6 months of opening the test strip vial
The Accu-Chek® Instant S blood glucose monitoring system helps to lower the testing barriers by supporting the ease-of-use with its components and features: TRI tool and USB connectivity to the Accu-Chek® Connect Online system. Instant clarity Get Instant clarity of your results in just a few seconds with a visual re-assurance. The intuitive 9 colour target range indicator helps you understand your results easily and know if they are above, in range or below range. Proven accuracy Guaranteed by the makers of the Accu-Chek products, fulfilling the requirements of the ISO 15197: 2013^ and delivering even tighter accuracy for reliable results you can trust. 1 button navigation Only what you need: Your test result and your averages (7/30/90 days) are visible on the meter. So there is no need to scroll through a menu to find what you need. 1 button is all it takes. No set up Simple preparation: No set up required ââ?¬ just insert a strip, apply a small blood sample, and read your blood glucose result on the large display. Remove the test strip after testing and the meter turns off automatically. Blood application Easy-edge blood dosing: A small blood sample can be applied anywhere on the wide, yellow edge of the test strip dosing area, that has a wide blood application area compared to leading brands. The test strip is designed to help make it easy to apply a small drop of blood on the end of the strip. * Blood glucose values (Lowsâ?¤69mg/dL, Normal 70-160 mg/dL, Highâ?¥161/dL) are pre-set on the Target Range Indicator and must be interpreted in conjunction with the appropriate medical condition at the time of taking reading, and in accordance with advice of your physician. ^ Criterion A of clause 6.3 for the lot tested (Freckmann et al., JDST, 6(5), 2012) # Figures refer to the TRI tool group of the study (n = 47) 1 Parkin CG, et al. Use of an Integrated Tool for Interpretation of Blood Glucose Data Improves Correctness of Glycemic Risk Assessment in Individuals With Type 1 and Type 2 Diabetes. J Diabetes Sci Technol
Accu-Chek Active Strip helps in determining the blood sugar level in the body. The sugar test strips absorb the blood easily and spreads quickly on the strip. The strips need a small amount of blood that shows reliable results in a few seconds. The kit includes Accu-Chek Active strips that can be used until the expiration date printed on the pack. After the test matches the colour of the strip visually to the closest coloured dot on the test strip container. The Acc-Chek strips are available in packs of 10, 25 and 50 strips. Benefits and Features accurate: Accurate1 blood glucose measurement easy: - No coding for even easier blood glucose monitoring - easy-to-read display (new typeface) - intuitive handling with just 2 buttons safe: - Underdose detection - visual double check - 10 seconds re-dose option clever: - Pre- and postmeal markers - postprandial reminder - 7,14,30 or now 90 day test averages - USB interface for data transfer
With XIENCE Sierra's new stent design, the XIENCE reputation now extends to offer unmatched deliverability, even with challenging complex lesions. ULTRA LOW STENT CROSSING PROFILE1 OF 0.039â?³ FOR EASIER CROSSING enabled by the new stent design and balloon technology1 XIENCE Sierra's exceptional deliverability also comes from the enhanced stent delivery system featuring a single-piece outer member for added pushability and trackability. Expanded Treatment Optionsâ?¡ With 5.5 mm post-dilatation capability for 3.5 mm and 4.0 mm stents, XIENCE Sierra can treat most large vessels. PROVIDES UNSURPASSED PRECISION IN PLACEMENT AND AVOID GEOGRAPHIC MISS zero shortening even at max expansion of 5.5 mm2 XIENCE SIERRA ENSURES COATING INTEGRITY3 even at max expansion XIENCE Sierra coating remains intact at maximum post-dilatation expansion of 5.5 mm from 3.5 mm XIENCE Sierra (3.5 x 18 mm) 25x magnification at max expansion of 5.5 mm XIENCE Sierra (3.5 x 18 mm) 150x magnification at max expansion of 5.5 mm Synergy coating shows multiple cracks with delamination at its max expansion of 4.25 mm from 3.5 mm Xience Xpedition represents a powerful combination of deliverability, strong clinical data and broad availability of meaningful sizes, three factors that make this product well-suited to treat a wide range of patients, The impact of the changes to the stent delivery system is particularly notable in patients with complex coronary anatomy. For these patients, physicians have a new technology to reach the blockage and restore blood flow with ease and confidence. In order to cater the variegated demands of our beloved clients, we are offering a wide range of Abbott Xience Xpedition Stent
As for Urine Reagent Analysis Strip Uncut Sheets , we have various parameters ranging from 1 to 12 . We can provide you strip and uncut sheet URS format with high quality and competitive price PRINCIPLE AND EXPECTED VALUES URS Ascorbic acid: This test involves decolorization of Tillmann's reagent. The presence of ascorbic acid causes the color of the test field to change from blue-green to orange. Glucose: This test is based on the enzymatic reaction that occurs between glucose oxidase, peroxidase and chromogen. Glucose if first oxidized to produce gluconic acid and hydrogen peroxide in the presence of glucose oxidase. The hydrogen peroxide reacts with potassium iodide chromogen in the presence of peroxidase. The extent to which the chromogen is oxidized determines the color which is produced, ranging from green to brown. Low amounts of glucose are normally excreted in urine.3 Glucose concentrations as low as 100 mg/dL, read at either 10 or 30 seconds, may be considered abnormal if results are consistent. At 10 seconds, results should be interpreted qualitatively. For semi-quantitative results, read at 30 seconds only. URS Bilirubin: This test is based on azo-coupling reaction of bilirubin with diazotized dichloroaniline in a strongly acidic medium. Varying bilirubin levels will produce a pinkish-tan color proportional to its concentration in urine. In normal urine, no bilirubin is detectable by even the most sensitive methods. Even trace amounts of bilirubin require further investigation. Atypical results (colors different from the negative or positive color blocks shown on the color chart) may indicate that bilirubin-derived bile pigments are present in the urine specimen, and are possibly masking the bilirubin reaction.
INTENDED USE The test kit utilize purified Chlamydia Trachomatis Antibody antigen, based on GIFA principle and use indirect method to detect Urea Plasma Urealyticum antibody in human serum. TEST PROCEDURE 1. Remove the test kit and put it at room temperature (for about 20-30mins) before testing. 2. Add 1 drop of Wash Buffer into the hole and allow the liquid soak the membrane completely. 3. Add 150l of the serum specimen into the hole and allow it to sufficient absorption. 4. Add 3 drops of Colloidal Conjugate into the hole and allow it to sufficient absorption. 5. Add 3 drops of Wash Buffer into the hole and allow it to sufficient absorption. Read the results within 3 minutes. STORAGE The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
INTENDED USE Feline Panleucopenia Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Panleucopenia Virus (FPV Ag) in cat's feces or vomit. PRINCIPLE OF THE ASSAY Feline Panleucopenia Virus(FPV) Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Panleucopenia Virus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Panleucopenia Virus antigen in the sample. INTERPRETATION OF RESULTS Positive: The presence of both C band and T band, no matter T band is clear or vague. Negative: Only clear C band appears. Invalid: No colored band appears in C zone, no matter whether T band appears. STORAGE The kit can be stored at room temperature (2-30�°C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
INTENDED USE Feline Immunodeficiency Virus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Immunodeficiency Virus antibody (FIV Ab) in cat's blood. PRINCIPLE OF THE ASSAY Feline Immunodeficiency Virus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody in the sample. INTERPRETATION OF RESULTS Positive: The presence of both C band and T band, no matter T band is clear or vague. Negative: Only clear C band appears. Invalid: No colored band appears in C zone, no matter whether T band appears. STORAGE The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
1. INTENDED USE FIV Ab + FeLV Ag Combined Rapid Test is a combined cassette to differentially diagnose the presence of Feline Immunodeficiency antibody and Feline Leukemia Virus antigen in cat's blood. Assay Time: 10-15 min Sample: serum, plasma or whole blood 2. PRINCIPLE OF THE ASSAY FIV Ab + FeLV Ag Combined Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody or FeLV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody or FeLV antigen in the sample. 3. KIT COMPONENT - 10 foil pouches, each containing a cassette,pipette and desiccant - 10 assay buffer tubes (0.5 mL each) - 10 centrifugal tubes - Product Manual
One Step Influenza A Test is a rapid qualitative assay that detects influenza type A (including the subtype H1N1) nucleoprotein antigen extracted from the nasal swab specimen. The device is used to aid in the diagnosis of influenza type A infection. For in vitro diagnostic use only. For professional use only. Influenza A SUMMARY Influenza (commonly known as flu) is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease that is easily transmitted through the coughing and sneezing of aerosolized droplets containing live virus. Influenza outbreaks occur each year during the autumn and winter months. There are three types of influenza viruses: A, B, and C. Only influenza A viruses are further classified by subtype on the basis of the two main surface glycoproteins hemagglutinin (HA) and neuraminidase (NA). Influenza A subtypes and B viruses are further classified by strains. Humans can be infected with influenza types A, B, and C viruses. Subtypes of influenza A that are currently circulating among people worldwide include H1N1, H1N2, and H3N2 viruses. Influenza B viruses can cause morbidity and mortality among humans, but in general are associated with less severe epidemics than influenza A viruses. Although influenza type B viruses can cause human epidemics, they have not caused pandemics. Influenza type C viruses cause mild illness in humans and do not cause epidemics or pandemics. Influenza A PRINCIPLE One Step Influenza A Test is a rapid immunochromatographic test for the visual detection of influenza type A antigen (nucleoprotein) extracted from the nasal swab specimen. The test adopts double antibody sandwich method. When the extracted specimen is added into the test device, the specimen is absorbed into the device by capillary action, mixes with antibody-dye conjugate, and flows across the membrane pre-coated with influenza type A monoclonal antibody. When the influenza type A antigen levels are at or above the target cutoff (the detection limit of the test), type A antigen in the specimen binds to the specific antibody-dye conjugate and are captured by influenza type A monoclonal antibody immobilized in the relative site of test region T of the device. This produces a colored test band in the test region. When the influenza type A antigen levels are zero or below the target cut off, there is not a visible colored band in the test region of the device. This indicates a negative result for influenza type A.
Intended Use The One Step HAV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Hepatitis A Virus (HAV) in Whole Blood /Serum / Plasma to aid in the diagnosis of Hepatitis A Virus. Summary Hepatitis A is an acute, usually self-limiting disease of the liver caused by hepatitis A virus (HAV). HAV is transmitted from person to person, primarily by the faecal-oral route. The incidence of hepatitis A is closely related to socioeconomic development, and seroepidemiological studies show that prevalence of anti-HAV antibodies in the general population varies from 15% to close to 100% in different parts of the world. One step HAV IgG/IgM Test is a simple, visual qualitative test that detects Hepatitis A Virus antibodies in human Whole Blood /Serum / Plasma. The test is based on immunochromatography and can give a result within 15 minutes. Principle The One Step HAV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis A Virus antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing HAV recombinant envelope antigens conjugated with Colloid gold (HAV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-HAV, T2 band is coated with antibody for the detection of IgG anti-HAV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-HAV, if present in the specimen, will bind to the HAV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a HAV IgG positive test result and suggesting a recent or repeat infection. IgM anti-HAV if present in the specimen will bind to the HAV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a HAV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
Syphilis Test INTRODUCTION 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. Syphilis Test LIMITATIONS The test is for in-vitro diagnostic use only.
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What are Crepe, Cohesive, Adhesive and Compression Bandages? A crepe bandage is a bandage made of light material (usually cotton, cotton & wool or rayon & cotton). It can be wrapped around different body parts and is used generally for sports and orthopaedic injuries such as cramps, sprains, strains, dislocation and aches. Why buy Crepe and Compression Bandages on Smart Medical Buyer Smart Medical Buyer stocks the widest range of Crepe Bandages online in India. We provide the lowest prices online, multiple payment options and same day dispatch for these products. What should one look at while buying crepe, compression, adhesive and cohesive bandages? * Colour of the bandage * Size of the bandage (length and breadth) * Part of the body part that the bandage needs to cover
General Information One-Step neisseria gonorrhoeae antigen test is detection of neisseria gonorrhoeae in female endocervical swab and male urethral swab specimens. Specimen: Swab/Urine Reading Time : 10-15 min
The One Step TORCH IgG/IgM Test is a panel of rapid qualitative lateral flow test designed for the quantitive detection of IgG and IgM antibodies to Toxoplasma gondii (TOXO), Cytomegalovirus (CMV), Rubella, Herpes Simplex Virus (HSV) in human serum/plasma samples.
