XH-22 Manual Lowering Device Detailed Product Description:· Manual Lowering Device has a unique braking system provides a constant, steady lowering speed.· Gears are large and tested to bear loads in excess of demand.· Castings are of non-corrosive aluminum and easy access to all internal working parts. · Ball bearings throughout for noiseless, smooth, and fully automatic operation.Technical Features:1.Packing Size: Main top:96*21*21cm, 96*21*21cm; 152*18*10cmSupport: 180*18*15cm, 100*30*24, 100*30*24cm, 180*18*15cm2.Gross Weightï¼?Support (one set): N.W: 57kg G.W: 60kgMain top (one set): N.W: 78kg G.W: 80kg Company FAQQuestion 1 What??s material of manual lowering device?Answer: Material is 304 Stainless SteelQuestion 2 Whether device can be adjusted according to body weight?Answer: Yes, tell factory requirements when give us an order.
XH-22 Manual Lowering Device for CemeteryDetailed Product Description:·Manual Lowering Device for Cemetery has a unique braking system provides a constant, steady lowering speed.·Gears are large and tested to bear loads in excess of demand.·Castings are of non-corrosive aluminum and easy access to all internal working parts. ·Ball bearings throughout for noiseless, smooth, and fully automatic operation.Technical Features:1.Packing Size: Main top:96*21*21cm, 96*21*21cm; 152*18*10cmSupport: 180*18*15cm, 100*30*24, 100*30*24cm, 180*18*15cm2.Gross Weight Support (one set): N.W: 57kg G.W: 60kgMain top (one set): N.W: 78kg G.W: 80kg
If "NOVOSYN VIOLETT" is a product or medical device, it may be associated with a manufacturer, such as a pharmaceutical or medical equipment company. To obtain the most accurate and up-to-date information, I recommend the following steps: Contact the Manufacturer: Try reaching out to the manufacturer associated with the product. They should be able to provide details about the product, its use, and any relevant specifications. Medical Professionals or Institutions: If you are a healthcare professional or associated with a medical institution, you may inquire within your organization for information about the specific product. Product Catalogs or Documentation: Check medical product catalogs, manuals, or documentation from relevant manufacturers or suppliers. This information is often available through official channels. Online Resources: Search online medical databases, catalogs, or supplier websites for the specific product code or name. Sometimes, product details are available on official websites or medical supply platforms.
Lot of 11 Portex 1st Response Adult Manual Resuscitator REF 8500 In original factory packaging & never used 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.
As the heart beats, blood forced through the arteries cause a rise in pressure, called systolic pressure, followed by a decrease in pressure as the heart's ventricles prepare for another beat. This low pressure is called the diastolic pressure. Sphygmomanometer measures this systolic/diastolic pressure in humans. DIALEX, an aneroid sphygmomanometer used to measure blood pressure is composed of an inflatable cuff to restrict blood flow and mechanical manometer to measure the pressure. Manual sphygmomanometer is used in conjunction with the stethoscope. FEATURES Dial BP monitor. Professional Quality. Mercury free. Clinically Accurate. Built to EN1060-1\2 Standards. Measurement Range 0-300mmHg. Sturdy and easy to transport, thus reliable both in professional and domestic use. DIALEX equipment complies with the European regulations in force in conformity with directive 93/42/EEC on medical devices Minimum Order Quantity 500 Piece Footprint Portable Is It LCD Display LCD Display Is It Portable Portable Individually packed Individually packed Patient Care Individually packed Mercury free Patient Care
Lot of 25 Mercury Medical CPR Bag Disposable Manual Resuscitators ISO 13485 In original factory packaging & never used Single patient use. 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 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.
1. INTENDED USE CDV + CPV Ag Combined Rapid Test is a combined cassette to diagnose the presence of Canine Disteimper virus antigen and Canine Parvovirus antigen in dogâ??s secretions, serum or feces. Assay Time: 5 - 10 min Sample: Secretions, serum or feces 2. PRINCIPLE OF THE ASSAY CDV + CPV Ag Combined Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CDV antigen or CPV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CDV antigen or CPV antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches each containing a cassette, pipette and desiccant - 10Ã?assay buffer tubes (0.7 mL each) - 10Ã?assay buffer tubes (1.0 mL each) - 20Ã?swab sticks - Product Manual
1. INTENDED USE CPV + CCV +Giardia Ag Triple Test is a combined cassette to differentially diagnose the presence of Canine Parvovirus antigen, Canine Coronavirus antigen and Giardia antigen in dogâ??s feces or vomit. Assay Time: 5-10 min Sample: Feces or vomit 2. PRINCIPLE OF THE ASSAY CPV + CCV + Giardia Ag Triple Test is based on sandwich lateral flow immunochromatographic assay. The test device has three testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CPV antigen, CCV antigen or Giardia antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV, CCV or Giardia antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing onecassette and a desiccant - 10Ã?assay buffer tubes (1.0 mL each) - 10Ã?pipettes - 10Ã?swab sticks - Product Manual
1. INTENDED USE CPV + CCV Ag Combined Test is a combined cassette to differentially diagnose the presence of Canine Parvovirus antigen and Canine Coronavirus antigen in dogâ??s feces or vomit. Assay Time: 5 -10 min Sample: Feces or vomit 2. PRINCIPLE OF THE ASSAY CPV + CCV Ag Combined Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough CPV antigen or CCV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV antigen or CCV antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing acassette, pipette and desiccant - 10Ã?assay buffer tubes (1.0 mL each) - 10Ã?swab sticks - Product Manual
1. INTENDED USE FIV Ab + FeLV Ag Combined Rapid Test is a combined cassette to differentially diagnose the presence of Feline Immunodeficiency antibody and Feline Leukemia Virus antigen in catâ??s blood. Assay Time: 10-15 min Sample: serum, plasma or whole blood 2. PRINCIPLE OF THE ASSAY FIV Ab + FeLV Ag Combined Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody or FeLV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody or FeLV antigen in the sample. 3. KIT COMPONENT - 10Ã?foil pouches, each containing a cassette,pipette and desiccant - 10Ã?assay buffer tubes (0.5 mL each) - 10Ã?centrifugal tubes - Product Manual