Lot of 10 Arrow Super Arrow-Flex Percutaneous Sheath Introducer Kit REF CP-07511-P EXP. 2012-07 In original factory packaging & never opened May be non-sterile due to expiration date Single patient use. New in original unopened factory package. Units are sold as non-sterile due to expiration of packaging. See pictures for more information. Not for human consumption. Not an implantable device. Items sold a non-sterile due to expiration of sterility on packaging are sold as-is and may be re-sterilized and used for training or veterinary purposes. "The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. Do not purchase this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item." DISCLAIMER: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by purchasing this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer. WAIVER LIABILITY AND INDEMNIFICATION AGREEMENT By placing this order with THE SELLER of this sale and accepting the parts, the purchaser agrees that the purchased materials or parts will be used solely at the purchaser's risk and that the purchaser will indemnify and hold THE SELLER, its owners and employees, free and harmless from all loss, liability and damage resulting from claims brought by any regulatory agencies, or by reason of any alleged failure or defect of any parts supplied by THE SELLER.
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Portable wireless oct devices, wireless oct devices, device for ophthalmology, device for dermatology, korean made portable oct scanner.
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Needle Destroyer
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.
General Information One-Step Beta lactam + Tetracycline Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Beta lactam and Tetracycline residue in milk. Specimen: Milk Reading Time : 5-10min
SUMMARY Bilirubin: This test is based on the coupling of bilirubin with a diazotized dichloroaniline in a strongly acid medium. The colors range from light tan to reddish-brown. Ketone: This test is based on the reaction of acetoacetic acid with sodium nitroprusside in a strongly basic medium. The colors range from beige or buff-pink color for a Negative reading to pink and pink-purple for a Positive reading. Specific Gravity: This test is based on the apparent pKa change of certain pretreated polyelectrolytes in relation to the ionic concentration. In the presence of an indicator, the colors range from dark blue or blue-green in urine of low ionic concentration to green and yellow-green in urine of higher ionic concentration. Blood: This test is based on the pseudoperoxidase action of hemoglobin and erythrocytes which catalyzes the reaction of 3,3, 5, 5-tetramethyl-benzidine and buffered organic peroxide. The resulting colors range from orange to yellow-green and dark green. Very high blood concentration may cause the color development to continue to dark blue. pH: This test is based on the well known double pH indicator method, where bromothymol blue and methyl red give distinguishable colors over the pH range of 5-9. The colors range from red-orange to yellow and yellow-green to blue-green. Protein: This test is based on the protein error-of-indicator principle. At a constant pH, the development of any green color is due to the presence of protein. Colors range from yellow for a �??Negative�?? reaction to yellow-green and green to blue-green for a �??Positive�?? reaction. Urobilinogen: This test is based on a modified Ehrlich reaction in which p-diethylaminobenzaldehyde reacts with urobilinogen in a strongly acid medium. Colors range from light pink to bright magenta. Nitrite: This test depends on the conversion of nitrate to nitrite by the action of Gram-negative bacteria in the urine. The nitrite reacts with p-arsanilic acid to from a diazonium compound in an acid medium. The diazonium compound in turn couples with 1,2,3,4-tetrahydrobenzo(h) quinolin to produce a pink color. Leukocytes: This test is based on the action of esterase present in leukocytes, which catalyzes the hydrolysis of an indoxyl ester derivative. The indoxyl ester liberated reacts with a diazonium salt to produce a beige-pink to purple color. Ascorbic Acid: The composition comprises of a complex chelating agent with a polyvalent metal ion in its higher state and an indicator dye that can reacts with the metal ion in its lower state to produce a color change from blue-green to yellow.
PRINCIPLE Progesterone (P4) is a kind of steroid hormone. The concentration change of P4 in milk is one specific characteristic indicating the activities of cow ovary. It plays an important role in the process of maternal reproduction and maintaining pregnancy. Therefore, it can be monitoring cow reproductive activity by detecting the concentration of P4. P4 concentration has different characteristic changes as the cow's stage of reproductive physiology, through to detect the progesterone levels can make an accurate diagnosis of cow in early pregnancy. PRODUCT FEATURES The strip can be used for diagnosis of cow early pregnancy, which is of high accuracy, easy operation, rapid and normal temperature storage, easy to carry, harmless to maternal and fetal safety. THE SCOPE OF USE The test is mainly suitable for dairy and beef cattle early pregnancy diagnosis, as well as to guide timely artificial insemination. THE BEST USE DATE Cow's estrus cycle is 21 days. There are individual differences in 18 to 24 days commonly, it is suggested to perform the test the 18th days after mating. Perform the test once every day for 5 continuous days; even if one negative result appears during the five days, which indicates the cow is not pregnant and P4 is at the lowest level at this moment. In this case, it was suggested to have the dairy cow mated in time; that should improve the conception rate. If positive results show for all 5 days tests, it indicates the cow is in pregnancy, and it should get careful nursing and gestation management. Another test method is to closely observe the cow rutting performance from 18 days after mating, if it was in rutting performance the detection should do immediately; for those that have no heat after mating to do a test on the 24th day. SPECIMEN COLLECTION 1.Milk sample: cleaning teats before take the milk, abandon to the first three milk, then collect milk in the bottle, take 1 ml in the test tube, placed the centrifuge10000 rpm for 10 minutes, in vitro milk sample was divided into three layers, using straws inserted in the underlying absorbing liquid cream and set aside. 2.Saliva: from the mouth collecting saliva for 3 to 5 ml placed the centrifuge 1500-2000 rpm for 5 minutes, take supernatant on standby. 3.The galley proof: from the hair root galley proof according to take 10 mg in the extracting pipe, add 3 ml anhydrous ethanol soak vortex shock 5 minutes after 2-3 hours, placed 3000 rpm centrifuge for 5 minutes, drain on ethanol solution 1 ml into glass dish, in 70-80 �?? oven dry reoccupy after 1 ml PBS dilution. Set aside. 4.Urine: can be used directly. 5.Blood: anticoagulant take 1 to 2 ml of centrifugal 2000 rpm 5-10 minutes from the plasma standby, the anticoagulant let stand for 30 minutes to separate serum blood clots. Set aside.
Home Menopause Test Strip is an in vitro diagnostic (IVD) qualitative test for rapid detection of human Follicle Stimulating Hormone (FSH) in urine at a sensitivity of 25mIU/ml. SUMMARY AND EXPLANATION OF THE TEST Follicle Stimulating Hormone (FSH) is a peptide hormone produced in the pituitary gland of the brain. It is normally present in the blood or urine varying in concentration with the stage of the menstrual cycle. When estrogen levels drop, FSH is released from the pituitary gland indicating that either a woman in mid-menstrual cycle or the onset of perimenopause. During early menopause, changes take place in the balance of hormones that regulate and control menstrual cycles. As a woman grows older and passes out of childbearing stage of life, the ovaries gradually make less of the hormone estrogen and FSH increases.FSH normally regulates the growth and development of an egg. Once this part of the monthly cycle is complete, FSH production is stopped and it returns to normal. As the body decreases estrogen production with age, more FSH is made. Over time these hormone changes cause menstrual periods to stop completely and "menopause" has occurred. The slow change in ovary function can happen between 2 and 10 years before the final period. This early stage before menopause is called perimenopause. During this stage, the levels of FSH may rise to positive levels and slowly return to normal, causing irregular or missed periods. The testing for FSH should be performed twice to help identify the levels of FSH throughout a menstrual cycle. PRECAUTION 1. For in vitro diagnostic use only. 2. Do not use after expiration date. 3. Test device should remain sealed until ready for use. Do not use if pouch is damaged or opened. 4. Read this instruction carefully before performing the test. 5. Do not re-use the test device. 6. Do not eat the desiccant in the pouch.
AMP INTENDED USE The AMP Gold Rapid Screen Test is a qualitative competitive binding immunoassay for determination of Amphetamine in urine. AMP PRINCIPLE The Amp Gold Rapid Screen Test is a chromatographic absorbent device in which drug or drug metabolites in a sample compete with drug antigen immobilized on a porous membrane support for limited antibody sites. Labeled antibody-dye conjugate mixes with sample specimen and binds to the free drug presented in sample forming an antibody-antigen complex. This complex prevents the formation of pink color bands in the test zone immobilized antigen conjugate when the drug is presented in the sample urine above the detection levels (1000ng/ml for Amphetamine). Unbound dye conjugate binds to the reagent in the control zone and produces a pink-rose color band, demonstrating that the reagents and device are functioning correctly. A negative specimen produces two distinct color bands, one for the control in the �¢??C�¢?? zone and one for Amphetamine in the �¢??T�¢?? zone. AMP REAGENTS AND MATERIALS PROVIDED 1. Test Device A pouched cassette contains a single test for Amphetamine 2. Dropper A transfer pipette seal in foil pouch together with test device 3. Operating Instructio MATERIALS REQUIRED BUT NOT PROVIDED AMP MATERIALS REQUIRED BUT NOT PROVIDED Packaging Details: Pouch+Box+Carton packaging (1) With our companyâ??s Logo (2) With the natural package (3) With OEM package (4) ODM Anna Lee Int'l Market Executive
General Information One-Step TB IgG/IgM Rapid Test is detection antibodies(IgG and IgM) anti-Mycobacterium Tuberculosis(M.TB) in human blood. Sensitivity :86.7% , Specificity : 90% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General information One-step cdv + cpv ag combined rapid test is a combined cassette to diagnose the presence of canine disteimper virus antigen and canine parvovirus antigen in dog’s secretions, serum or feces. Sensitivity : cdv 100% cpv 99.3% Specificity :cdv 99.8% cpv 99.4% Specimen: secretions, serum or feces Reading timen:5-10 min
General information Feline infectious peritonitis virus ag test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of fip-triggerred coronavirus antigen(fcov ag) in cat’s feces, serum and ascites. Assay time: 10 - 15 min Sample: mixture of serum and feces extraction, ascites or secretions
General information Method: double antibodies sandwich method Sensitivity : 100% Specificity : 99.8% Specimen : ocular and nasal secretions, serum, plasma Detection limit: 101.9 tcid50 / 0.1 ml No cross reaction against cpv, ccv, civ, cpiv Reading time : 5- 10 min
General information One-step cow pregnancy rapid test is to improve milk output and shortening the period of non-pregnancy. Analytical sensitivity : 2ng/ml Sensitivity : 96.9% , specificity : 97.8% Specimen : milk Reading time : 5 min No cross-reactivity: fsh (100g/ml), e2(10g/ml), prl(100g/ml), lh(25miu/ml), dht(10g/ml), tetraborane(10g/ml) and h2o.
General information One-step tumor marker rapid test is an immunochromatography based one-step in vitro diagnostics test for the qualitative determination of afp, psa and cea in human serum or plasma. Afp : alpha-feto protein test to detect liver cancer Psa : prostate-specific antigen test to detect prostate cancer Cea : carcinoembryonic antigen test to detect colorectal cancer Specimen : serum or plasma Reading time : 20 min
