![]() None of the information on this page has been provided or approved by Eximo. While we have made attempts to ensure that the information displayed are correct, Zippia is not responsible for any errors or omissions or for the results obtained from the use of this information. ![]() Sources of data may include, but are not limited to, the BLS, company filings, estimates based on those filings, H1B filings, and other public and private datasets. The data on this page is also based on data sources collected from public and open data sources on the Internet and other locations, as well as proprietary data we licensed from other companies. The employee data is based on information from people who have self-reported their past or current employments at Eximo. This type of complaint will continue to be monitored for trends.Zippia gives an in-depth look into the details of Eximo, including salaries, political affiliations, employee data, and more, in order to inform job seekers about Eximo. G) if the auryon catheter cannot be advanced in this attempt, stop the laser activity, withdraw the auryon catheter and use a new catheter.Ī review of the angiodynamics complaint system noted no adverse trends for this complaint type and product family. When advancement resumes, you should stop self-count-down and resume it if additional non-advancements are experienced.ī) if the auryon catheter cannot be advanced by the 10th second of laser activation, you should release the foot switch to stop the laser, retract the catheter approximately 3-4 mm, and try to advance again while rotating the catheter shaft approximately 90 degrees to either side, while resuming 10 seconds count down.Ĭ) if the auryon catheter is still not advancing with the above-mentioned rotation manipulation for the additional 10-seconds, immediately stop the laser activity by releasing the footswitch.ĭ) ask the laser operator to raise the fluence to the 60mj/mm2.Į) activate the laser and try again to advance the auryon catheter through the lesion.į) if the auryon catheter cannot be advanced, resume the self-count-down to 10 seconds. Self-count-down should start the moment you experience non-advancement of the auryon catheter. If you experience any difficulty to advance the auryon catheter, immediately start self-count-down. Once this gw is angiographically verified to cross the lesion in the vessel's lumen, it is ready for auryon catheter insertion over the wire.Īdvancement of auryon catheter through the lesion: a) do not to exceed 10 seconds of lasing at the same location. Inadvertent movement of the catheter may result in patient injury.Īlways use fluoroscopic surveillance when advancing the auryon catheter inside the patient vasculature to avoid misplacement, dissection, or perforation.Īuryon catheter insertion over the wire until laser activation: you may use any other gw to cross the lesion, but the final gw that auryon catheters will track over should be 300cm 0. Labeling review: instructions for use is provided with the catheter device and contain the following statements: warnings: pay careful attention while using the catheter, avoid excessive force and be on alert for any potential damage. ![]() ![]() The lot/serial number of the catheter used was not reported by the end user, therefore, adevice history records review could not be performed. Without receiving the catheter sample for evaluation a root cause for this event cannot be determined. The customer's reported complaint of catheter melted coating of guidewire cannot be confirmed since the catheter sample was not returned. As the reported defective device was not returned, angiodynamics is unable to perform a device evaluation. ![]()
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