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LED work light, LED daytime running light, hid work light, hid driving light / LED, hid search light, HID remote control search light, hid kits, hid ballast.
40W CREE LED Work Lights_SM-620 . Power: 40W . Voltage: DC 9-50V . LED: 4PCS*10W (USA CREE LED) . Size: 125*155*88 mm . 30000 hours above life time . LED Color Temperature: 5000K, 6500K, 8000K . Waterproof rate: IP68. Product Feature: 1. SM-620 has good waterproof & dustproof function. 2. SM-620 LED work light back cover and front cover can be apart; easy to install and change. 3. The shell of the lights is made of high-pure aluminum alloy, electrostatic coating, thermostatic hardening and excellent adhesion. 4. Introduce USA CREE LED. Size: 125*155*88 mm, Weight: 1.45KGS.
25W CREE LED Work Lights_SM-613 . Power: 25W . Luminous flux: 2050 LM . Size: 116*63mm . LEDs: 1pcs*25W (CREE LEDs) . Life Time: 30000 hours . Waterproof: IP67 ( clear water 3 meters ) Product Feature: 1. Small size, may actually assemble with the combination of wide range of applications, CREE 10W LED, low power consumption, high luminous flux. 2. Small installation dimensions. 3. Number of pods can be used with the heght and width. 4. Can withstand heavy use from the elements. Net Weight: 0.7KG Packaging: 1pcs/box,20pcs/carton.
This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens. This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical reference only and cannot be used as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patients should be considered in combination with their symptoms/signs, medical history, other laboratory tests and treatment responses. Positive test result needs to be further confirmed, negative result does not preclude 2019-nCoV infection. This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures. TEST PRINCIPLE The kit is immunochromatographic and uses double-antibody sandwich method to detect 2019-nCoV N protein antigen. During detection, the treated specimens are loaded into the sample wells of the test card. When the concentration of 2019-nCoV antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies first. Under chromatography, the complexes move forward along the nitrocellulose membrane till captured by pre-coated monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to form a pink/purple reaction line on the detection zone, at this point the result is positive; conversely, if there is no viral antigen or the concentration of antigen in specimen is below the minimum detection limit, no pink/purple reaction line appears in the detection zone, at this point the result is negative. Regardless of whether the sample contains viral antigens or not, a pink/purple reaction line will appear in the quality control zone (C), the pink/purple reaction line that appears in the quality control zone (C) is the criterion for determining if the chromatography process is normal.
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