hibiscus is a bleach of important beverages in winter. The bleaching of the margins are used to slimming and remove the fat as it 1 - the body of the amount of overloading as it urges the urine that helps in 2 weight of weight. 3 - Method of mutation, causing weight loss. 4 - The malicious cholesterol rate in the body is motivated by weight loss normally. 5 - Diagnostic helps to burn the inmissal fat in the body. 6- The most prominent benefits of the hibiscus to the body's abduction prevention from carbohydrate storage as limits absorbed. 7 - Diagnosis is reduced from the amount of adult affairs to his ability to reinforce the appetite .... He also has other benefits like: 1 - the painful accompanying the monthly cycle and reduces the products that wipe down the abdomen. 2 - To restore hormone transportation, which relieves the symptoms accompanying the monthly cycle, such as over-eating and mood. 3 - increase the body resistance to diseases such as flu and cold, as the maintenance of the immune system is available to contain the hibernite of high alcohcic acid in addition to the characteristics of 4-to-theatal bacteria and infections. 5 - Flipher of fever. 6_eselillis eclipse process. 7 - Wizard constipation. 8-alternative urine. 9 Body of the risk of rectal cancer and colon cancer. 10 - Soter of neurosuff, fighting anxiety if drinking is drinking before bedtime to contain it for natural chemical vehicles that give the relaxation of the body. 11. The high blood pressure level. 12. Keep the health of the liver and stimulates it to perform his functions as protecting from the risk of fatty liver and lobby. 13 Free the root of the roots in the body for its weight antioxidant. 14. Keep the health of the brain and contribute to the revitalization of neurons. 15 - The blood circulation in the body commanded in maintaining the health of the heart . Power Herpes products are distinguished by being natural, organic products that are not exposed to any chemicals.
The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples. Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients. The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.
Uncut Sheet Strep A IgG/IgM Rapid Test Format:Cassette/Strip Uncut Sheet A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only. INTENDED USE The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection. SUMMARY Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4 The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen. PRINCIPLE The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.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. 2.The test must remain in the sealed pouch until use.
Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
Detailed introduction to XPS Board-X300: Our Corporation introduces the most advanced automated production lines all over the world. The computer pre-stores thousands of process parameters, equipped with full automatic control of various processes, automatic fault inspections and diagnosis closed recycled material processing system, various plate on-line automatic control and adjustment, the programs above are under network control by three country expert groups, which solves the quality non-stability phenomenon caused excess operators. Properties: Model: X300 Thermal Conductivity W/(m.K): 0.023-0.028. Compressive strength (kPa): 300. Nominal Density (kg/m3): 32-35. Fire behavior: Class E. Oxygen Index (%): 27-33. Applicable temperature: Minus 50¡ãC-Positive 75¡ãC Max. Size (mm): 2400*1200*150. Surface: Smooth planing, embossing & slotting, peel removal. Edge: Flat, lap joint, tenon, rain gutter. Application: Heat preservation & insulation for building, floors, parking platforms, and other moisture-proof insulation etc. Key Features: Ø Able to resist repeated freeze/thaw cycles. Ø High density, tough and durable, not easily damaged. Ø Dimensionally stable, cryogenic secondary foaming. Ø Flame-retarded, light weight, thermal bridge breaker, easy to install. Ø ECO, ODP, GWP: zero Ozone Depletion Potential, low global warming potential, the 1st manufacturer which uses CO₂ foaming technology in China, each piece of insulation board dedicates love for global environmental protection causes. As required.
Nano Seha is a powerful replacement for traditional chemical or acid disinfecting and sterilization processes. The product uses 100% natural elements and has been repeatedly proven to be safe for humans yet lethal against all of the pathogens. Our Products are approved By US FDA accredited labs & DM and US Patented Technology. Our products are ideal for daily and frequent use in Hospitals, Airports, Railway stations & all public places. These are ideal for personal use as well. INGREDIENTS:100 % Natural,� Effectiveness: up to 24 hours , SHELF LIFE:3 years, Bacterial Reduction:99.9999% Reduction Aloe vera: a light, almost transparent green fragrance, with rejuvenating, healing, or soothing properties. Strawberry: A favorite amongst children, a fragrance that spells just fruity. Oud Noora: Undoubtedly a fragrance that evokes pure luxury and exclusivity, with long-lasting persistence on the skin. These variants are available in all sorts of packing.
Product Name - REALY TECH" Rapid Coronavirus Antigen Test (SARS-Cov-2) Product Description - Specifications Test duration: 15 minutes Sample type: nasopharyngeal swab. Storage: at room temperature or refrigerated (2-30A' C) Expiration: 24 months ex works Performance characteristics Sensitivity: 96.72%. Specificity: 99.22%. Accuracy: 98.74%. Price of product ( USD price or FOB price) - DEPENDS ON QUANTITY Product origin - China Key Specifications/Special Features - 5 test boxes: Each test box is packed in an aluminum foil bag with desiccant. 5 extraction reagents: vial with 0.3 ml extraction reagent 5 sterilized swabs: disposable swabs for sample collection 5 extraction tubes 5 dropper tips 1 work station 1 leaflet Minimum Order Size and Packaging details - MOQ 30000 units
Product Name - Realy Tech" Rapid Coronavirus Antigen Test (sars-cov-2) - Product Description - Specifications Test duration: 15 minutes Sample type: nasopharyngeal swab. Storage: at room temperature or refrigerated (2-30 C) Expiration: 24 months ex works Performance characteristics Sensitivity: 96.72%. Specificity: 99.22%. Accuracy: 98.74%." Product origin - China Key Specifications/Special Features - 25 test boxes: Each test box is packed in an aluminum foil bag with desiccant. 25 extraction reagents: vial with 0.3 ml extraction reagent 25 sterilized swabs: disposable swabs for sample collection 25 extraction tubes 25 dropper tips 1 work station 1 leafle
* This product has a painted finish that is uniform in colour, gloss, texture & thickness, with excellent paint adhesion and durability. Coils can be readily rollformed, bent, pressed, cut, drilled, lock-seamed and stamped without degradation in the quality of the paint CONSTRUCTION Cladding/siding, Roofing, Sliding shutter, Building accessories, Doors, Partitions, Canopies of gas stations, False ceiling, Prefabricated buildings, Sandwich panels, Bill boards HOUSEHOLD APPLIANCES Washing (washing machine & tumble dryer), Cooking (oven & microwave oven), Cold (Refrigerator, freezer, visi cooler, water cooler), Electric Application (griller, toaster, air conditioner) TRANSPORT Railway carriages, Bus-body building, Lorrycintainers, License plate, Dash boards, Road signs INDUSTRY / MISCELLANEOUS Containers, Packaging, Aerosol, Clock Dials, Furniture, Light Fixtures, Cooking Utensils, Computer & Peripherals.
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.
INTENDED USE The One Step RV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Rubella (Virus) in Whole Blood /Serum / Plasma to aid in the diagnosis of RV infection. The test is based on immunochromatography and can give a result within 15 minutes. PRINCIPLE The One Step RV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of RV antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing RV recombinant envelope antigens conjugated with Colloid gold (RV 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-RV, T2 band is coated with antibody for the detection of IgG anti-RV, 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-RV, if present in the specimen, will bind to the RV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a RV IgG positive test result and suggesting a recent or repeat infection. IgM anti-RV if present in the specimen will bind to the RV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a RV 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 (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
FlexiShine Pollyblends has launched a next-generation technology to create glass-filled PP compounds. We create compounds with unprecedented strength. Glass Filled PP Compound is prepared by compounding Polypropylene Homo-Polymer with a fine grade of glass. The entire process followed as par the industry standard and up to mark of all grades which are suggested by the authorities. Glass-Filled PP Compound manufacturers in India use a special technique to increase the long term thermal-mechanical properties. We use some additives like antioxidants, lubricant, processing aid. It shows good dispersibility and excellent balance of properties in the final product if some compounds are used directly or diluted with desired grades of polypropylenes. FEATURES High strength High chemical resistance High melting point (150 to 200F) Very low density Abrasion resistance Lightweight Low-cost fabrications Machinable Maintenance-free Weldable Wipes clean Dimensional stability Excellent electrical properties Typical Applications Acid Tank/Lineup Battery Cases Tank Covers Etching Machines/Rinse Tubes Machined Parts Fume Hoods Ducts Scrub Stations Metal Plating Barrel
Specification: 1,This cable is produced according to the standard BS6500,IEC60227:1993, VDE 0281 2,BS6360 Class 5,Solid or Stranded Bare Copper Conductor 3,BS7655 TI 1PVC Insulation 4,PVC Sheathed, color available Application: The cable is suitable to be fixed wireing of power device,power lighting of home electric equipment and instrument, inner wiring of electric enquipment Instrument, electron equipment, automatization device etc. Suitable for use in conduit and for fixed, protected installation of Wiring Burglar Alarm, Public Address Systems,Intercoms, Telephone Stations, Speakers, Instrumentation, Control and other Low Voltage Circuits that are Power Limited and anti-interference needed Product Feature: Linecorenumberand conductornominalsection Conductor Constructionn/mm Norminalthinkness ofinsulation(mm) Overall Diameter(mm) At20DCResistanceof conductor(Ω/km) 1.5 30/0.25 0.7 3.05±0.05 13.3 2.5 77/0.20 0.8 3.65±0.05 7.98 4.0 56/0.30 0.8 4.25±0.08 4.95 6.0 84/0.30 0.8 5.25±0.08 3.30 Factory Presentation&Certificate
Specification: 1,This cable is produced according to the standard BS6500,IEC60227:1993, VDE 0281 2,BS6360 Class 5,Solid or Stranded Bare Copper Conductor 3,BS7655 TI 1PVC Insulation 4,PVC Sheathed, color available Application: The cable is suitable to be fixed wireing of power device,power lighting of home electric equipment and instrument, inner wiring of electric enquipment Instrument, electron equipment, automatization device etc. Suitable for use in conduit and for fixed, protected installation of Wiring Burglar Alarm, Public Address Systems,Intercoms, Telephone Stations, Speakers, Instrumentation, Control and other Low Voltage Circuits that are Power Limited and anti-interference needed Product Feature: Linecorenumberand conductornominalsection Conductor Constructionn/mm Norminalthinkness ofinsulation(mm) Overall Diameter(mm) At20DCResistanceof conductor(Ω/km) 1.5 30/0.25 0.7 3.05±0.05 13.3 2.5 77/0.20 0.8 3.65±0.05 7.98 4.0 56/0.30 0.8 4.25±0.08 4.95 6.0 84/0.30 0.8 5.25±0.08 3.30 Factory Presentation&Certificate
Specification: 1,This cable is produced according to the standard BS6500,IEC60227:1993, VDE 0281 2,BS6360 Class 5,Solid or Stranded Bare Copper Conductor 3,BS7655 TI 1PVC Insulation 4,PVC Sheathed, color available Application: The cable is suitable to be fixed wireing of power device,power lighting of home electric equipment and instrument, inner wiring of electric enquipment Instrument, electron equipment, automatization device etc. Suitable for use in conduit and for fixed, protected installation of Wiring Burglar Alarm, Public Address Systems,Intercoms, Telephone Stations, Speakers, Instrumentation, Control and other Low Voltage Circuits that are Power Limited and anti-interference needed Product Feature: CONDUCTOR INSULATION COVERING MAX.COND. RESISTANCE (Ω/km,20°C,DC) DIELECTRIC STRENGTH (VAC,1min) AWG CONSTR- UCTION (No./mm) DIA. (mm) INSULATION THICKNESS (mm) O.D. (mm) JACKET THICKNESS (mm) O.D. (mm) 28 7/0.127 0.38 0.46 1.30 0.40 2.10 239 2,000 26 7/0.16 0.48 0.46 1.40 0.40 2.20 150 2,000 24 11/0.16 0.61 0.49 1.60 0.40 2.40 94.2 2,000 22 17/0.16 0.76 0.47 1.70 0.40 2.50 59.4 2,000 20 26/0.16 0.94 0.48 1.90 0.40 2.70 36.7 2,000 18 41/0.16 1.18 0.46 2.10 0.40 2.90 23.2 2,000 16 26/0.254 1.49 0.46 2.40 0.40 3.20 14.6 2,000 14 41/0.254 1.88 0.46 2.80 0.40 3.60 8.96 2,000 Factory Presentation&Certificate
Water Activated Sandless Self-Inflating Flood Bags FLOODBLOC is a small, light-weight package that makes a big difference in both consumer and commercial settings for defending public, residential and rural areas from water damage caused by flash flooding by diverting water flow. FLOODBLOC will easily contain and control large amounts of water and moving water. Our design allows you to quickly transport large quantities of bags when you need them, while the strip format allows for rapid deployment of barriers over long stretches with ease. FLOODBLOC outperforms traditional sandbags in every way imaginable. From their weight to their ability to easily conform to objects next to them. You can rely on FLOODBLOC to keep water where it should be. With easy deployment FLOODBLOC products can prevent the disastrous financial aftereffects of water damage caused by flooding. This includes flooding and water damage to commercial buildings, homes, shops, parking garages, as well as creating issues for traffic and transit. Using FLOODBLOC products can also effectively increase the recovery time after such periods of flooding and heavy rainfall seasons. Specific examples of use include: street diversions, road entry, street intersections, housing community entrances, shelters, bridges, bridge underpasses, underground parking, basements, store and home fronts - yards - gardens, commercial buildings and structure exteriors, side-walks, driveways, parkway and roadway exits, farm land, rural roads, highway/ parkway shoulders, train and bus stations and stops, airport structures, streets with gradients, city parks and public areas, construction zones, dig sites etc. FLOODBLOC is superior to sand-filled bags in every way from storage, transport, creation and function MODULAR DESIGN FLOODBLOC is available in single bags, strips of five, and strips of ten. Block style bags bags are perfect for stacking and connecting to form barrier walls to divert heavy flowing or standing water during times of flooding. Modular strip style bags are great for covering larger areas in short periods of time. Easy to deploy, the bags are laid down and activated when coming in contact with water. Bags inflate and becomes a water barrier with the exact same functional property of standard commonly used sand filled bags. Thousands of bags can be delivered to areas of need in a small vehicle (vs. only 15 - 20 sand filled bags). Bags can last several months once they are activated and are 100% eco-friendly and biodegradable. Unactivated bags can be stored for several years.
Specification: 1,This cable is produced according to the standard BS6500,IEC60227:1993, VDE 0281 2,BS6360 Class 5,Solid or Stranded Bare Copper Conductor 3,BS7655 TI 1 PVC Insulation 4,PVC Sheathed, color available Application: The cable is suitable to be fixed wireing of power device,power lighting of home electric equipment and instrument, inner wiring of electric enquipment Instrument, electron equipment, automatization device etc.  Suitable for use in conduit and for fixed, protected installation of Wiring Burglar Alarm, Public Address Systems,Intercoms, Telephone Stations, Speakers, Instrumentation, Control and other Low Voltage Circuits that are Power Limited and anti-interference needed Product Feature: Model No. Conductor Insualtion Jacket Cores � Nom. Area Max. Resistance at 20°C Thickness Min. Resistance at 70°C Thickness Min. Dia. Max.  mm² MΩ/km mm MΩ/km mm mm mm RVV2�0.75 2�0.75 26 0.6 0.011 0.8 6 7.6 RVV2�1.0 2�1.0 19.5 0.6 0.01 0.8 6.4 8 RVV2�1.5 2�1.5 13.3 0.7 0.01 0.8 7.4 9 RVV2�2.5 2�2.5 7.98 0.8 0.009 1 8.9 11 RVV3�0.75 3�0.75 26 0.6 0.011 0.8 6.4 8 RVV3�1.0 3�1.0 19.5 0.6 0.01 0.8 6.8 8.4 RVV3�1.5 3�1.5 13.3 0.7 0.01 0.9 8 9.8 RVV3�2.5 3�2.5 7.98 0.8 0.009 1 9.6 12 RVV4�0.75 4�0.75 26 0.6 0.011 0.8 6.8 8.6 RVV4�1.0 4�1.0 19.5 0.6 0.01 0.9 7.6 9.4 RVV4�1.5 4�1.5 13.3 0.7 0.01 1 9 11 RVV4�2.5 4�2.5 7.98 0.8 0.009 1.1 10.5 13 RVV5�0.75 5�0.75 26 0.6 0.011 0.9 7.4 9.6 RVV5�1.0 5�1.0 19.5 0.6 0.01 0.9 8.3 10 RVV5�1.5 5�1.5 13.3 0.7 0.01 1.1 10 12 RVV5�2.5 5�2.5 7.98 0.8 0.009 1.2 11.5 14 Factory Presentation&Certificate FAQ Q1. What kind of products can your company supply?  A: We specialize in supplying network cable, coaxial cable, HDMI cable, VGA cable, telephone cable, speaker cable and ect.  Q2. What's your MOQ? A: The MOQ of long meter cable is 50 km, or we can negociate.  Q3. What's your delivery time? A: Our delivery time is about 15-20 days after comfriming the deposite, it is based on the quantity of the order.  Q4. What are your payment terms? A: Normally, we accept T/T in advance, as for other payment term, we can negociate with you.  Q5. What's your trade term ? A: We can accept FOB, CIF, EXW term.   Q6. What's your conventional packing ? A: 100m/plastic or wooden drum, 305m/wooden drum or color box. However, we can produce according your demand.  Q7. Can your factory customize cables based on clients' samples or data sheet ?  A: Yes, we can .
