Product name: hCG One Step Pregnancy Test Kit,FSH One Step Menopause Rapid Test Kit ect. Specimen: Urine Format: Strip/cassette/midstream Specification: 25pcs, 40pcs, or customized MOQ: 10,000 pcs Accuracy: > 99% Storage: 4-30°C Valid for: 24 months
Product name: TORCH IgM Rapid Combo Test Device Format: Cassette Specimen: Whole blood/serum/plasma Test items: Toxo IgM, CMV IgM, Rubella IgM, HSV 1 IgM, and HSV 2 IgM Valid for: 24 months 2.Features -Customized sensitivity, printing color and packing -Accurate, quiet, stable, convenient -Latest production -Competitive quality and price -Easy payment and shipment
Multi-drug one step 2-15 drug test device (urine/saliva) 1.Product description 15.Png 20170120153542.Png Give a rapid diagnosis for reference to help in hospitals & clinics, rehabilitation centers, diseases control & prevention centers, military recruiting, high-risk group census, physical examination and some related special industries. Urine or saliva specimen to choose, easy specimen collection Instant result in 5 minutes Ce marked Valid for 24 months. Store at 2-30, 2.Features -choices: urine or saliva specimen for multi-drug test -test more than 2 drugs in one time, distinct c/t lines -customized sensitivity, printing color and packing -accurate, specific, quiet, stable, convenient -latest production -best seller in china domestic market, competitive quality and price -easy payment and shipment
Flu A H5 subtype Antigen Rapid Test Kit/Flu A H7 subtype Antigen Rapid Test Kit/Flu A H9 subtype Antigen Rapid Test Kit. They're highly sensitive, high specificity, and it's easy to use. Because the company is manufacturer, we can offer better quality at reduced prices.
This rapid test kit is to detect p80 protein specific antibody of bvdv, which is accurate, sensitive and specific.
Nebulizer Mask Direction For Use: 1, Place prescribed medication in nebulizer jar by unscrewing lid. 2,Reattach lid. 3,Place the mask on the patientâ??s face, centering both nose and mouth. The elastic strip should be below the ears and around the neck. 4,Gently pull the ends of the strap to adjust. Adjust metal strip at bridge of the nose to secure fit. 5,Attach nebulizer connection to face mask connection. Cautionï¼? 1ï¼?For single use. Discard after use. 2ï¼?Do not use if package is open or damaged. 3ï¼?Do not store at extreme temperature and humidity. Store in cool and dry place. Ensure that all connections are secure and air circulates freely through the tubing.
(1)The One Step Drug Screen Test Panel (Urine) is an immunoassay based on the principle of competitive binding.Drugs which may be present in the urine specimen compete against their respective drug conjugate for binding sites on their specific antibody. (2)During testing,a urine specimen migrates upward by capillary action. A drug, if present in the urine specimen below its cut-off concentration, will not saturate the binding sites of its specific antibody coated on the particles. The antibody coated particles will then be captured by the immobilized drug conjugate and a visible colored line will show up in the test line region of the specific drug strip. The colored line will not form in the test line region if the drug level is above its cut-off concentration because it will saturate all the binding sites of the antibody coated on the particles.
1.Product description (1)Product name: hCG One Step Pregnancy Test Kit (2)Specimen: Urine (3)Format: Strip/cassette/midstream (4)Specification: 25pcs, 40pcs, or customized (5)MOQ: 10,000 pcs (6)Accuracy: > 99% (7)Storage: 4-30°C (8)Valid for: 24 months
A rapid test for the qualitative detection of antibodies (IgG and IgM) to Dengue virus in whole blood, serum, or plasma. For professional in vitro diagnostic use only. INTENDED USE The Dengue IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum, or plasma as an aid in the diagnosis of primary and secondary Dengue infections. DIRECTIONS FOR USE Allow the test device, specimen, buffer, and/or controls to reach room temperature (15 30°C) prior to testing. 1.Bring the pouch to room temperature before opening. Remove the test device from the sealed pouch and use it as soon as possible. 2.Place the test device on a clean and level surface. For Serum or Plasma Specimens: Hold the dropper vertically, draw the specimen up to the Fill Line (approximately 5 μL), and transfer the specimen to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 L) and start the timer. See illustration below. Avoid trapping air bubbles in the specimen well (S). For Whole Blood (Venipuncture/Fingerstick) Specimens: To use a dropper: Hold the dropper vertically, draw the specimen 0.5-1 cm above the Fill Line, and transfer 1 drop of whole blood (approximately 10 µL) to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 uL) and start the timer. See illustration below. To use a micropipette: Pipet and dispense 10 µL of whole blood to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 µL) and start the timer. See illustration below. 3.Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.
A rapid test for the qualitative detection of circulating antigens of Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae in whole blood. For professional in vitro diagnostic use only. Sensitivity The Malaria P.f/ Pan Rapid Test Device (Whole Blood) has been tested with thin or thick microscopy on clinical samples. The results show that the sensitivity of the Malaria P.f/ Pan Rapid Test Device (Whole Blood) is >99.9% relative to microscopy. For Pan: Relative Sensitivity: >99.9% (158/158) (97.6%100.0%)* For P.f: Relative Sensitivity: >99.9% (53/53) (93%100.0%)* Specificity The Malaria P.f/ Pan Rapid Test Device (Whole Blood) uses highly specific antibodies for Malaria P.f/ Pan antigens in whole blood. The results show that the specificity of the Malaria P.f/ Pan. Rapid Test Device (Whole Blood) is over 99.0% relative to microscopy. Relative Specificity: >99.0% (324/327)(97.3%99.8%)* Accuracy: >99.4%(535/538)(98.3%99.8%)* * 95% Confidence Interval Total Results211327538 Note: The comparison for Pan line has been only done with blood specimens positive with Plasmodium vivax specimen. The claims for Pan lines are based on scientific findings that Pan-malarial Aldolase is found in other malarial parasites including Plasmodium ovale and Plasmodium malariae.
Troponin I (CTnI) One Step Rapid Test Kit (Whole blood/serum/plasma) Product description Product name: CTnI One Step Troponin I Rapid Test Kit Specification: Lateral-flow Immunofluorescence Chromatographic Assay 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Type: Cassette MOQ: 10,000 PCS Analytical Range: 1.0~50ng/ml (Whole Blood); 0.1~50ng/ml (Serum/Plasma) Specimen: Human serum/plasma/whole blood Manufacturer: Hangzhou Laihe Biotech Co., Ltd. 2.Clinical significance (1)Diagnosis of various chest pain (2)Foundation of ACS diagnosis and risk stratification (3)Best markers for ACS prognosis (4)An aid in the diagnosis of myocardial infarction (injury) (5)Can improve clinical, economic and operational outcomes
In One Cup Cup Multi-drug One Step 2-15 Drug Test Simple Cup (Urine) CE Qualified (MOP/MET/KET/AMP/BAR/BUP/BZO/COC/COT/MDMA/THC/MTD/OPI/PCP/TCA)
Disposable nebulizer Item no: MO-1 Place of Origin: Danyang, China MOQ: 5000pcs Supply Ability: 200,000pcs/month Port: Shanghai, Ningbo etc Be light in weight, comfortable for carrying and using; Made of medical grade PVC, 100% latex free; Universal connector(luer lock) is available; Different size of atomizing cup can meet the needs of different clinical atomizing time; Smooth and feathered edge for patient comfort and reducing irritation points; Sterilized by EO gas if needed; Stature meter, Disposable nebulizer, Disposable oxygen masks Factory
Ningxia Biyuan Activated Carbon Co., Ltd. sells carbon additive for sale anthracite coal for metallurgy carbon additive carbon, which is finished by series production process. The appearance of black, granular, with developed pores, good adsorption properties, high strength, economic advantages, product features and application range: high fixed carbon content, low sulfur content, stable oil effect, high carbon absorption rate, degree of graphitization The best is to increase the nucleation of molten iron, which is mainly used for smelting cast steel and cast iron. Ningxia Biyuan Activated Carbon Co., Ltd. is a professional manufacturer and has about eight years of different filter media production and domestic historical trade. Now we are committed to developing our international trade. We adhere to the principle of "integrity management, quality service". Our employees are professional and sincere, and our prices are fair. Look forward to working with you.
TB/T 3237 Chinese Fire test standard for railway vehicles - Standard TB/T 3237 Flame retardant technical specification of decorating materials for multiple unit train TB/T 3237 Chinese Fire test standard for railway vehicles Test Method GB 2406 Oxygen index test UIC 564 Combustion test GB 8323 Smoke density test TB 3237 Part 4.4 Smoke toxicity test TB/T 3237 Chinese Fire test standard for railway vehicles Scope This Standard is applicable to the flame retardant decorating materials for the multiple unit train with an operation speed larger than or equal to 200km/h. This Standard specifies the flame retardant property requirements and test methods for the decorating materials for multiple unit train. TB/T 3237 Chinese Fire test standard for railway vehicles Reference Standard GB/T 2406.2 Plastics - Determination of Burning Behavior by Oxygen Index GB/T 10707 Rubber - Determination of the Burning GB/T 8323.2 Determination of Optical Density by a Single-chamber Test UIC 564-2 Regulations relating to fire protection We also can provide the following service of fire test to Railway EN45545-2 Fire protection of railway vehicles: Requirement for fire behaviors of materials EN45545-3 Fire resistance requirements for fire barriers NFPA 130 Standard for fixed guideway transit and passenger rail systems DIN5510-2 Fire behaviour of materials and parts, classification, requirement and test methods BS6853 Code of practice for fire precautions in the design and construction of passenger carrying trains NF F16-101 Railway Rolling Stock Fire Behavior Choice of Material
Rail transit is one of the main means of transportation. Because of its limited space, it is difficult to escape. The fire performance of materials of railway vehicle has attracted more and more attention around the world. There are two main standards of fire protection for railway vehicle, EU standard EN45545 and NFPA130. EN 45545 Standards EN 45545-2 Requirement for fire behaviors of materials and components Fire Hazard LevelHL1HL2HL3 Product CategoryR1 R26 Test MethodISO5658-2ISO5660-1 ISO9239-2 ISO4589-2ISO5659-2NFX70-100 EN 45545-3 Fire resistance requirements for fire barriers NFPA 130 American Standard NFPA 130 Standard for fixed guideway transit and passenger rail systems Test Items Surface Flammability, Smoke Density, Heat Release Test method
( 1) Electric control cupboard: The electric box remains in the form of plastic splashing, and the strength and sturdiness are improved, and the covering will not break. Built-in security electronic control system, fully compliant with CE common operating system. ( 2) Gear box: The transmission is constructed from top notch actors iron product, with reduced noise and excellent shock absorption. The integrated gear revolves, which has high rotation efficiency as well as lengthy life span compared with the conventional belt equipment. ( 3) Upper box: Integrated die plate as well as pushing roller, premium alloy steel is utilized to improve the life span. Different die plate designs are suitable for various materials to guarantee the important result. What are the benefits of chicken feed pellet making device What are the benefits of a chicken pellet making equipment Equipment's feed pellet device generates high temperature and high pressure during the pressing procedure, the feed has a strong paste fragrance, and also the feed appearance is hard, which satisfies the qualities of gnawing animals of chicken, poultries, pigs, cattle and sheep, as well as boosts the palatability of the feed. Easy to consume, the nutrient absorption conversion rate is raised by 300%, safe as well as clean and sterile, the quantity of the straw is doubled after pelleting, which is convenient for long-term storage space and transportation. ( 1) Basic structure, wide applicability, small impact as well as reduced sound. ( 2) Powdered feed and also yard powder can be granulated without (or a little) liquid addition. Therefore, the moisture web content of pelleted feed is generally the dampness web content of the product prior to pelleting, which is a lot more conducive to storage. ( 3) The pellets produced by this hen pellet making equipment have high solidity, smooth surface and also sufficient internal healing, which can enhance the food digestion and absorption of nutrients, as well as can eliminate general pathogenic microbes and also bloodsuckers. It appropriates for elevating bunnies, fish, ducks and also laboratory animals., which is a lot more affordable than blended powder feed. ( 4) This SZLH hen pellet making device model is geared up with 1.5-12mm diameter mold and mildews, which are suitable for granulation of various materials and attain the best result. ( 5) Adjust to different materials to make certain the pressing impact. Compression molding of wood chips, corn stalks, etc needs a great deal of stress. In the very same kind of chicken feed pellet making equipment, the roller part is the main part of the whole devices, and the top quality alloy steel is used to enhance the service life of the roller.
OVERVIEW Many power systems, railway systems, large-scale petrochemical plants and enterprises have a lot of electrical equipment whose internal insulation are mostly oil filled insulation type, and therefore, test on insulating oil dielectric strength is common and necessary. To meet the needs of the market, we have developed and produced a series of insulating oil dielectric strength testers according to national standard GB T507-2002, industry standard DL429.9 91 and the latest Electric Power Industry Standard DL T846.7-2004 by ourselves. This instrument, by using a single chip microcomputer as the core, can operate in full automation with high accuracy, greatly improving work efficiency and reducing the labor intensity of workers. Moreover, it is small in size and convenient to carry. MAJOR TECHNICAL INDICATORS Output voltage 0 100KV optional Voltage distortion rate 3 Voltage raising speed 0.5 5 KVS adjustable Standing time 15min adjustable Boosting interval 5 min adjustable Boosting frequency 1 9 time s optional Booster capacity 1.5KVA Measuring accuracy 3 Supply voltage AC220V 10 50Hz1 Hz Power 200W Applicable temperature 0 45 Applicable humidity 75 RH Overall dimension 465 385 425 Transformer Oil Dielectric Strength Tester 2
Hernia Mesh Hernia mesh is made of medical grade polypropylene monofilament, and diamond mesh is woven on the knitting machine by changing the pulling density. Hernia mesh is made of medical grade polypropylene monofilament, and diamond mesh is woven on the knitting machine by changing the pulling density. Hernia mesh is an absorbable and non-degradable material. The hernia mesh is a single-strand structure, which ensures that the mesh edge should not be leaked, and the position is fixed and stable. It fully meets the requirements of implant materials. The mesh of hernia mesh has large inter-mesh pore. It is not suitable to hide bacteria in the mesh. It has strong resistance to infection and can effectively stimulate the proliferation of fibrous tissue, which is conducive to tissue growth and healing. The hernia mesh has good histocompatibility, fast acting with fibrin gel in the body, effective adhesion and fixation with tissue, forming a strong barrier, and no tension exists, effectively preventing hernia recurrence. In recent years, with the rapid development of material science, hernia mesh has been widely used in clinical practice, making a fundamental change in the treatment of hernia. The operation is usually completed in about half an hour. Local anesthesia is a minimally invasive operation. Application of hernia mesh: tension-free hernioplasty for primary inguinal and femoral hernia. square and oval hernia meshes with different sizes and specifications for customers to choose from.
1.Extra soft, durable wet wipes with a touch of soothing aloe are ideal for everyday clean-ups and incontinence care. 2.The ph-balanced, hypoallergenic and alcohol-free wipes provide exceptional skin care. 3.Single patient use wipes help to reduce the risk of cross contamination. 4.Do not flush wipes in the toilet. 5.Scented or Frag Free. 6.Application for all Over Body or Body-Perineal.
