China New Product Electric Standing Desks B for Orlando Factories

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Maximum load 120kg Maximum speed 38mm/s Height Adjustable Range 690-1170mm Frequency of use 10% max. 2 min – 18min on/off Ambient temperature: O℃ and 40℃ Color Grey, black, white Function Through the controller settings button   Can remember four height

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The business upholds the philosophy of "Be No.1 in high-quality, be rooted on credit and trustworthiness for growth", will keep on to serve previous and new prospects from home and overseas whole-heatedly for Acid Picking , Adjustable Computer Desk , Stand Up Desk , In case you are interested in almost any of our products and solutions, be sure to feel cost-free to contact us for additional aspects. We hope to cooperate with additional good friends from everywhere in the earth.
China New Product Electric Standing Desks B for Orlando Factories Detail:

Maximum load


Maximum speed


Height Adjustable Range


Frequency of use

10% max. 2 min  18min on/off

Ambient temperature:

Oand 40




Through the controller settings button


Can remember four height

Product detail pictures:

China New Product 
 Electric Standing Desks B for Orlando Factories detail pictures

We are proud in the significant client satisfaction and wide acceptance due to our persistent pursuit of top quality both on merchandise and repair for China New Product Electric Standing Desks B for Orlando Factories, The product will supply to all over the world, such as: Sri Lanka , Croatia , Mongolia , As an experienced manufacturer we also accept customized order and we could make it the same as your picture or sample specification. The main goal of our company is to live a satisfactory memory to all the customers, and establish a long term business relationship with buyers and users all over the world.

  • Tandem MIG is a dual wire, high productivity GMAW process designed for flexible robotic or
    fixed hard automation welding applications. The process utilizes high-speed inverter
    Waveform Control Technology™ to coordinate two separately generated GMAW welding
    arcs in unison for exceptional process flexibility. Independent control of both the lead and
    trail wire parameters of the tandem process allows procedure optimization for bead wetting,
    bead profile and penetration. Tandem MIG has proven to frequently double the production of
    single GMAW processes.

    Adam Slivka, MD, PhD, Associate Chief, Clinical Services Division of GI, Hepatology & Nutrition; University of Pittsburg Medical Center, demonstrates the Zilver® Biliary Self-Expanding Stent



    INTENDED USE: This device is used in palliation of malignant neoplasms in the biliary tree.

    STENT DESCRIPTION: This stent is an open-ended cylinder of nitinol. The design of the stent resists radial compression and easily conforms to bends in the bile duct anatomy without collapsing. There are radiopaque markers on each end of the stent to assist in fluoroscopic visualization of the stent position.

    DELIVERY SYSTEM DESCRIPTION: The stent is compressed onto a flexible delivery system. The delivery system accepts a .035 inch wire guide.

    NOTES: Do not use this device for any other purpose than the stated intended use.

    If the package is opened or damaged when received, do not use. Visually inspect with particular attention to kinks, bends and breaks. If an abnormality is detected that would prohibit proper working condition, do not use. Notify Cook for return authorization.

    Store in a dry location, away from temperature extremes.

    CONTRAINDICATIONS: Contraindications include those specific to ERCP and any procedure to be performed in conjunction with stent placement.

    Additional contraindications include, but are not limited to: inability to pass the wire guide or stent through the obstructed area, biliary duct strictures of benign etiology, biliary obstruction preventing either endoscopic or percutaneous cholangiography, concurrent perforated bile duct, those patients for whom endoscopic or percutaneous procedures are contraindicated, patients with coagulopathy, concurrent bile duct stones, strictures greater than 8 cm in length, and any use other than those specifically outlined under Intended Use.

    POTENTIAL COMPLICATIONS: Potential complications associated with ERCP include, but are not limited to: pancreatitis, cholangitis, aspiration, perforation, hemorrhage, infection, sepsis, allergic reaction to contrast or medication, hypotension, respiratory depression or arrest, cardiac arrhythmia or arrest.

    Additional complications that can occur in conjunction with biliary stent placement include, but are not limited to: trauma to the biliary tract or duodenum; obstruction of the pancreatic duct; stent migration; tumor ingrowth, tumor overgrowth of stent ends, or excessive hyperplastic tissue ingrowth.

    PRECAUTIONS: Refer to the package label for the minimum channel size required for this device.

    This stent must be placed under fluoroscopic monitoring.

    This stent must only be placed using the delivery system provided with the set.

    This stent is intended for palliative treatment only. Alternate methods of therapy should be investigated prior to placement.

    After stent placement, alternate methods of treatment such as chemotherapy and irradiation should not be administered as this may increase the risk of stent migration due to tumor shrinkage, stent erosion, and/or mucosal bleeding.

    Long-term patency with this stent has not been established. Periodic evaluation of the stent
    is advised.

    If the wire guide or stent cannot advance through the obstructed area, do not attempt to place the stent.

    Assessment must be made to determine the necessity of sphincterotomy or balloon dilation prior to stent placement. In the event sphincterotomy or balloon dilation is required, all appropriate cautions, warnings and contraindications must be observed.

    WARNINGS: This stent is not intended to be removed. Attempts to remove the stent after placement may cause damage to the surrounding mucosa. This stent is considered to be a permanent implant.

    This device is not intended to be deployed through the wall of a previously placed or existing metal stent. Doing so could result in difficulty or inability to remove introducer.

    A complete diagnostic evaluation should be performed prior to placement to measure the stricture length and determine the proper stent length.

    The safety and effectiveness of this device for use in the vascular system has not been established.

    The stent contains nickel, which may cause an allergic reaction in individuals with nickel sensitivity.

    In China, we have many partners, this company is the most satisfying to us, reliable quality and good credit, it is worth appreciation.

    5 Stars By Karen 2016-8-29 15:42
    We are long-term partners, there is no disappointment every time, we hope to maintain this friendship later!

    5 Stars By Sara 2016-2-24 14:25

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