Wholesale Lot of 13 Arrow-Clark Pleura Seal Thoracentesis Kits REF AK-01000 EXP. 2013-12 May be non-sterile due to expiration date Single use only. Brand new in original unopened factory package. See pictures for more information. Not for human consumption. Not an implantable device. "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 no 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.
Lot of 12 Various Kits 1 Arrowgard Blue Large-Bore Multi-Lumen CVC Kit REF. CDC-22123-1A EXP. 2013-08 1 Pneumothorax Kit REF. AK-01500 EXP. 2013-03 1 Pressure Injectable Multi-Lumen CVC Kit REF. CDC-15703-P1A EXP. 2013-10 1 Large-Bore Multi-Lumen CVC Kit REF. CDC-25123-1A EXP. 2012-10 2 Arterial Line Kits REF. AK-04510-S EXP. 2013-03 2 Radial Artery Catheterization Kits REF. AK-04020 EXP. 2013-07 4 Pediatric Multi-Lumen Central Venous Catheterization Set REF. CS-16553-J EXP. 2013-01 isclaimer 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.
Seal Kit
Iwp high pressure seal kit is utilized compound materials by precise processing. Related with pressuer, water flow, water quality, and temperature, Its longevity is between 300-1000hours. Working pressure in 380mpa. Wearable and maintaince easily.
IWP seal kit for lp for ceramic plunger is a set of seals, Its longevity could be reaching 2000hours at first time to use.And up to 3000hours after replacement. Recommend to replace seals in half year, twice in a year to keep machinery effectively.
INTENDED USE The Malaria Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Plasmodium falciparum (Pf) antigen in whole blood. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with Plasmodium. Any reactive specimen with the Malaria Rapid Test must be confirmed with alternative testing method(s) and clinical findings. STORAGE Store the test kits at room temperature 4- 30 degrees C. The sealed pouch has a self life of 24 months.of transmitting disease.
The GENEDIA W COVID-19 Ag is an in vitro diagnostic single-use test and qualitative immunoassay to detect SARS-CoV-2 antigen in nasopharyngeal swab and sputum specimen from human. This assay is designed for professional personnel in laboratory and at point-of-care as an aid in screening patients suspected of being infected and asymptomatic patients. Allow wider testing with fast test time (10 minutes) Clinically proven data of asymptomatic patients available Separately packed extraction solution to minimize the possibility of contamination No additional instruments required Package Unit : 20 Tests/Kit Expiration Date : 24 Months (while sealed in the original aluminum foil pouch) GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva The price is negotiable according to the amount of your order and shipping term. No MOQ is required but we prefer 1 pallet with 9,600 tests. (20 tests/kit, 30 kits/carton, 16 cartons/pallet)
INTENDED USE The Malaria Gold Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of antibodies including IgG, IgM and IgA to Plasmodium falciparum (Pf) and vivax, ovale, and malariea (Pv.o.m) in whole blood. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with Plasmodium. Any reactive specimen with the Malaria Gold Rapid Test must be confirmed with alternative testing method(s) and clinical findings. REAGENTS AND MATERIALS PROVIDED 1. Each kit contains 25 test devices, each sealed in a foil pouch with three items inside: a. One cassette device. b. One plastic dropper. c. One desiccant. 2. Sample diluent (1 vial, 5 ml) 3. One package insert (instruction for use). MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer 2. Lancing device for whole blood test
One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces) Cat. No.: RH0301T INTENDED USE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing. PRINCIPLE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary. STORAGE The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch. WARNING AND PRECAUTIONS 1. For in vitro diagnostic use only. 2. Do not use kit beyond the expiration date. 3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures. 4. The test device should not be reused. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. One operating Instruction MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer SPECIMEN COLLECTION AND PREPARATION 1. Collect stool sample by using the sample collection device provided. 2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample. 3. Put the sample collection stick back in the sample collection device and screw together tightly. 4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing. ASSAY PROCEDURE 1. Remove the test device from foil pouch by tearing along the notch. 2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION 3. Shake the sample collection device several times. 4. Holding the sample collection device upright, carefully unscrew the tip of collection device. 5. Squeeze 2-3 drops of the sample solution on the test sample pad. 6. Read the test results in 5 minutes. INTERPRETATION OF RESULTS Negative: Only one colored band appears on the control region (C). No colored band in the test region (T). Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T). Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.
1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma. 2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures. 3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens. 4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. Test Procedure Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) prior to testing. 1. Bring the pouch to room temperature before opening it. 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. 3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below. 4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes. Interpretation of Results Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is. Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region. Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
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.
BOSON RAPID SARS CoV-2 Antigen Test Card (Self Test) Manufactured by Xiamen Boson Biotech Co., Ltd. DHSC - UK Approved - 3rd Phase Approved. NASAL TEST CE & ISO Approved Full Home Test - Self Test Approval for UK and Europe Test Result in 15 Minutes. Sensitivity 97.70% Specificity 99.84% Accuracy 98.97% Layperson study statistics 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly Each Test have Unique Identifier Number - Easy to track Approved By - UK, Germany, France, Spain, Netherlands, Greece, Belgium, Italy, Portugal. 1 Test / Kit Catalog No.: 1N40C5-2 Kit Components: 1 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 1 sterilized swab 1 extraction tube 1 sample extraction buffer IFU Tube holder on back of box Box / Carton Specifications : 1 Test / Kit Box size - 190*60*15 mm Carton size - 42*42*33 cm Carton gross weight - 9.9 kg 250 tests (boxes) / carton Euro 1.12
BOSON - Rapid SARS-CoV-2 Antigen Test - Pack of 5 Available at 0.75 EUR Plus VAT and Transport per test IFU - Swedish, Finissh, Norwagian, English, Danish Product Descirption : "A home test for the rapid qualitative detection of SARS-CoV-2 virus antigen in anterior nasal swabs from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 Performance Characteristics: Sample type: nasal swab Time to result: 15-20 min Sensitivity - 97.70% Specificity - 99.84% Accuracy - 98.97% UK MHRA - DHSC Approved for Self Test Approved in Germany, France, Italy, Belgium, Netherlands, Greece, Spain, Portugal. Layperson study statistics: 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly Test Kit Specifications: 5 Tests / Kit Catalog No.: 1N40C5-4 Kit Components: 5 Rapid SARS-CoV-2 Antigen Test Card (sealed foil pouch) 5 sterilized swabs 5 extraction tubes 5 sample extraction buffer IFU 1 tube stand Box / Carton Specifications : 5 Tests / Kit Box size - 202*60*37 mm Carton size - 42*42*33 cm Carton gross weight: 10 kg 500 tests (100 boxes) / carton" MOQ : 3000 FOB Price : Euro 1.03
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.
Lot of 5 Arrow Injectable Multi-Lumen CVC Kit REF CDC-45703-XP1A EXP. 2012-11 Single use only. Brand new in original unopened factory package. See pictures for more information. Not for human consumption. Not an implantable device. "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 no 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.
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