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INTACEPT MACOS DOWNLOAD INSTALL

To avoid the risk of electric shock, the RFG must be connected only to a supply mains with protective earth.Doing so could lead to electromagnetic interference and possible death. DO NOT use the Relievant RFG on patients with implantable pulse generators (e.g., pacemakers, defibrillators) or other electronic device implants.

INTACEPT MACOS DOWNLOAD INSTALL

Install the RFG in a room that complies with all locally applicable requirements (including and not limited to IEC, CEC, and NEC) for safety and electromagnetic compatibility of high-frequency electrical surgical equipment.

Failure to follow these instructions may result in product damage.

Pay close attention to the care and cleaning instructions in the RFG maunal.

Refer any readjustments, modifications, and/or repairs to Relievant Medsystems or its authorized representatives.

Attempt no internal repairs or adjustments not specifically detailed in the RFG manual.

Federal law (USA) restricts this device to use by, or on order of, a physician.

The Probe may interfere and adversely influence the operation of other electronic equipment.Failure of the RFG could result in an unintended increase of output power to the Probe.Read and understand the Instructions For Use (“IFU”) completely prior to use.Improper surgical use and technique may lead to suboptimal clinical outcomes. Physicians using the Intracept System should be familiar with the physiology and pathology of the selected anatomy to be treated and be trained in the performance of the chosen surgical technique. Do not use the Intracept System or Relievant RFG (RFG) if you have not been properly trained in its use.Reconditioning, refurbishing, repair or modification of the device to enable further use is prohibited.Re-sterilization or reuse may result in cross contamination, patient infection, or device malfunction. Do not re-sterilize or reuse Intracept System.Do not use the Intracept System after the expiration date has passed as product integrity and/or sterility may be compromised.Do not use the Intracept System if package is opened or damaged as product integrity and/or sterility may be compromised.Application with electrosurgical instruments NOT tested and specified for use with the Relievant RFG.Situations where unintended tissue damage may result, based on the clinical assessment by the physician.Patients with implantable pulse generators (e.g., pacemakers, defibrillators) or other electronic implants.Skeletally immature patients (generally ≤ 18 years of age).Patients with active systemic infection or local infection in the area to be treated.Patients where the targeted ablation zone is Patients with severe cardiac or pulmonary compromise.Use of the Intracept Intraosseous Nerve Ablation System (Intracept System) is contraindicated in: