Air cleaner safety element 60123505 Suitable for Sany Excavator Truck SY35 As a leading supplier of parts suitable for construction and mining equipment we provide SDLG, XCMG, SANY, LIUGONG, LGMG and TONLY OEM parts
Smokeless garbage incinerator.
Portable Air Purifier, Negative/plasma Ion Generator, Ozone Generator.
Esp, air cleaners, electrostatic precipitators, smoke filter.
The wireless remote control grab is a kind of bulk grab that can be applied to the single cable grab in the air. It is usually used with a single-hook crane, which solves the difficulty of traditional single cable grabs with low working efficiency and large operation intensity. For single-hook type cranes and ship cranes, its work is reliable and easy to operate. The grapple comes with a closed hydraulic system. The wireless remote control device is used to realize the opening and closing of the grab. It not only has the characteristics of simple structure and reliable use of the rope grab, but also has the characteristics of high production efficiency of the power grab. It is widely used in ships, ports, stations, factories, mines and other industries. It is an ideal tool for handling bulk cargoes such as coal, mineral powder, bulk chemical fertilizers, and yellow sand. The wireless remote control grab can work under harsh environment such as high temperature, cold, dust, rain, etc. and its performance is not affected. The remote control distance can reach more than 100 meters. The grab uses high-performance battery. After each charge, the grab can be Continuous operation for more than 100 hours. Connection to the crane: The balancer of the grab can be used directly on the hook of the crane.
3D geomat for erosion control and slope protection Specification: 1)Erosion control mats 2)Polyethylene (PE) 3)Tensile strength:0.8 ~ 3.5kn/m. 4)220-480g/m2 5)thickness:10~20mm Features: It is a kind of high polymer synthetic material made of 3D mesh structure, 3D geomat, quality of a material is loose, flexible, with 90% of the space can fill soil,sand,the roots of the plants are grown through them balanced, the growth of grass make gauze pad, turf, soil surface firmly together, because the plant roots can be extended into the surface of the 30-50 cm, so the formation of a solid layer of green composite coating. Application: 1. Before the greensward grows, 3D GEOMAT prevents the surface of the land from the erosion of the wind and rain. 2. Form compound protection layer with the vegetable, standing the wash-out of the high water level and large speed current. 3. Replace the concrete, asphalt, and block, using in the slope surface protection of roadway, railway, river-way, dyke, and the hillside, etc. 4. For erosion control and slope protection of dams, river banks, channels, landfill and pond edge protection.
Basic Parameters Bus Power Supply: 9 32VDC Current consumption (static) 14mA FF/PA 11V 35 VDC(HART) Input Signal: Pt100, Pt1000, Cu50, Cu100 , 0, 0 to 500 4000 Resistance, B, E, J, N, K, R, S, T eight degrees of Thermocouple, -100mV 100mV Voltage Signal The Channel Number: Single Channel Fieldbus Protocol: FF/PA/HART wih CE Insulation: Between the Terminal and the Housing 500Vrms(707VDC) Operating Temperature: 40 85 Humidity Range: 0% 95%RH Starting Time: 5secs. Turnover Time: 0.5secs. Electromagnetic Compatibility: In Line with the GB/T 18268-2010 Explosion-Proof Sign: Ex ia IIC T4 Ga (HART)
Temperature Controller.
TV Remote Control & Battery.
Rfid tag access control.
Thermostats.
Temperature controller, electromagnetic relay, time relay, time controlled switch, present counterm, protector.
Thermostat.
Sample Types : Including Nasopharyngeal swab, Oropharyngeal swab, Sputum Controls : Internal control, UNG enzyme and dUTP used to reduce risk of contamination, false positive and false negative results Product Information Upper and lower respiratory specimens such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate. Authorized Laboratories Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. About Emergency Use Authorization (EUA) This test (1) has not been FDA cleared or approved, (2) has been authorized by FDA under an EUA for use by authorized laboratories, (3) has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and (4) is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C.360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
Indication: Qualitative detection of nucleic acid from SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider. Emergency use of this test is limited to authorized laboratories. Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. This letter is in response to your1 request that the Food and Drug Administration (FDA) issue an Emergency Use Authorization (EUA) for emergency use of your product,2 pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. 360bbb-3). On February 4, 2020, pursuant to Section 564(b)(1)(C) of the Act, the Secretary of the Department of Health and Human Services (HHS) determined that there is a public health emergency that has a significant potential to affect national security or the health and security of United States citizens living abroad, and that involves the virus that causes COVID-19. Pursuant to Section 564 of the Act, and on the basis of such determination, the Secretary of HHS then declared that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19 subject to the terms of any authorization issued under Section 564(a) of the Act. Having concluded that the criteria for issuance of this authorization under Section 564(c) of the Act are met, I am authorizing the emergency use of your product, described in the Scope of Authorization of this letter (Section II), subject to the terms of this authorization. I. Criteria for Issuance of Authorization I have concluded that the emergency use of your product meets the criteria for issuance of an authorization under Section 564(c) of the Act, because I have concluded that: 1. The SARS-CoV-2 can cause a serious or life-threatening disease or condition, including severe respiratory illness, to humans infected by this virus; 2. Based on the totality of scientific evidence available to FDA, it is reasonable to believe that your product may be effective in diagnosing COVID-19, and that the known and potential benefits of your product when used for diagnosing COVID-19, outweigh the known and potential risks of your product; and, 3. There is no adequate, approved, and available alternative to the emergency use of your product. 4 II. Scope of Authorization I have concluded, pursuant to Section 564(d)(1) of the Act, that the scope of this authorization is limited to the indication above.
The COVID-19 RT-PCR Detection Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C. 263a, to perform high complexity tests. Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper and lower respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infective status. The agent detected may not be the definite cause of disease. Positive results do not rule out bacterial co-infection with other viruses. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The COVID-19 RT-PCR Detection Kit is intended for use by qualified trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR Detection Kit is only for use under the Food and Drug Administration's Emergency Use Authorization. PRINCIPLE OF DETECTION This product is a fluorescent probe-based Taqman RT-PCR assay system. Firstly, the RNA of SARS-CoV-2 will be reverse transcribed into cDNA by reverse transcriptase, and then PCR amplification will be performed with cDNA as template. During amplification of the template, the TaqMan probe will be degraded due to the 5'-3 polymerase activity and exonuclease activity of Taq DNA polymerase, then the separation of fluorescent reporter and quencher enables the fluorescent signal to be detected by instrument. The ORF1ab gene of SARS-CoV-2 will be detected qualitatively by FAM channel, the N gene of SARS-CoV-2 will be detected qualitatively by JOE channel, the E gene of SARS-CoV-2 will be detected qualitatively by ROX channel, and the internal reference will be detected by CY5 channel. dUTP and UNG enzyme are used in the kit to prevent contamination of the amplified products. Internal reference is used in the kit for quality control starting from sample collection
Temperature controls and thermostats.
Ceiling fan and light IR remote control.
Magnetic Pointer Rail Thermometer is used to measure the temperature of rail. rail thermometer is not only dedicated to measure the temperature of the railway rails, but also can measure the air temperature and the surface temperature of other objects.
Place of Origin:CHINA Material:Stainless Steel Application:Construction Machinery Color:Sliver Warranty:1 Year MOQ:1 Pieces Type:Fittings Packaging & Delivery Selling Units:Single item Single package size: 20X8X8 cm Single gross weight:0.500 kg Package Type:normally packing
