MEDTRONIC SINGLE CHAMBER TEMPORARY PACEMAKER - CHD Medical

Medtronic 5348 Single Chamber Pacemaker Temporary Patient Monitor *USED*

medtronic single chamber pacemaker 5348

Venue Address North Hiatus Road. Due to the variability among sterilizers, precise sterilization instructions must come from the sterilizer manufacturer. During connection and testing procedures, only battery-powered instrumentation should be used.

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Application of temporary high-rate pacing should be performed under careful patient monitoring and control. Indications, Safety, and Warnings Read More. Preparation for use Connector Setup Figure When not in use, the ring and the bails fold flat against the back of the device. Buyer is responsible for all dismantling, rigging, crating, loading:

Atrial high-rate burst pacing therapy is intended for use in the atrium only. High-rate burst pacing in the ventricle may result in life-threatening arrhythmias. The temporary pacemaker is MR Unsafe.

Monitor the patient continuously while the temporary pacemaker is in use to ensure it is operating properly and delivering appropriate therapy to the patient. ECG monitoring should be in use and defibrillating equipment should be placed on standby and be kept immediately available during pacing lead insertion, pulse generator connection and adjustment, measurements of stimulation thresholds or sensed potentials, and application of antitachycardia burst therapy.

Use of high rates in the atrium may result in accidental conduction to the ventricle. Defibrillation equipment should be kept immediately available during high-rate pacing.

Operational failure of the temporary pacemaker can occur as the result of battery depletion, mishandling, or random component failure. Complications related to the use of temporary external pacemakers such as the Model include, but are not limited to asystole following abrupt cessation of pacing, inhibition, and reversion.

Potential complications related to the use of pacing lead systems with the Model include, but are not limited to myocardial irritability resulting in fibrillation, infarction, pericarditis, rejection, muscle and never stimulation, and infection. Complication related to inhibition or reversion of the pacemaker in the presence of strong electromagnetic interference. Whenever possible, for the safety of the patient, disconnect the temporary pacemaker from the implanted lead system before defibrillating or cardioverting.

Excessive defibrillation energy can damage the temporary pacemaker. This can result in a large current flowing through the implanted lead system and temporary pacemaker, which could reduce intended defibrillation energy delivered to the patient or cause myocardial damage.

A lead with extension cable constitutes a direct, low-resistance current path to the myocardium. During connection and testing procedures, only battery-powered instrumentation should be used.

Extreme caution must be taken to properly ground all line-powered equipment used in the vicinity of the patient. Electrosurgical units can cause tachyarrhythmias by inducing current on the leads.

Improper connection, displacement or fracture of leads or cables may result in pacemaker system failure. Inspect leads and cables for damage before each use. The pacing lead system may cease to function at any time due to improper connections or lead-related problems such as displacement or fracture. Do not modify the temporary pacemaker. Modifications could impact the temporary pacemaker effectiveness and adversely affect patient safety.

Federal law USA restricts this device to sale by or on the order of a physician. The Medtronic Model Single-Chamber Temporary Pacemaker is intended to be used in conjunction with a cardiac pacing lead system for temporary single chamber pacing in a clinical environment by trained personnel. The external pacemaker is designed for temporary stimulation of the heart in case of rhythm disturbances and conduction defects.

According to present clinical experience, the instrument is especially suited for stimulation of the heart in the following cases:. There are no contraindications with regards to the use of the for temporary cardiac stimulation for therapy and prevention of arrhythmia. The state of health of the patient, however, can restrict the choice of operational mode and stimulation parameters.

For example, a mode of operation with atrial sensing is not suitable or appropriate when atrial fibrillation occurs. This is due to the excessive and chaotic frequency of detected fibrillation waves.

Overdrive-stimulation therapy must only be used in the atrium. This item is USED and may contain defects that are not immediately detectable. Text description given is meant to be used as a guide only. You are responsible for inspecting item before bidding. All information provided is believed to be correct but NO warranty as such is either intended or implied. If you cannot meet removal requirements please refrain from bidding.

Buyer is responsible for all dismantling, rigging, crating, loading: Sign in or Register. There are 6 available at the time of this listing. Unit was test with a 9V battery. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on 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. 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 bidding on this equipment, indicates their acknowledgement of, and agreement to the terms of this disclaimer.

Bilder: medtronic single chamber pacemaker 5348

medtronic single chamber pacemaker 5348

Atrial pacing is ineffective in the presence of atrial fibrillation or flutter. Asynchronous pacing is contraindicated in the presence of intrinsic cardiac rhythms.

medtronic single chamber pacemaker 5348

Unit was test with a 9V battery. Page 36 The ventricular output ranges from 0.

medtronic single chamber pacemaker 5348

Complications related to the use of temporary external pacemakers such as the Model include, but are not limited to asystole following abrupt cessation of pacing, inhibition, and reversion. Remove Subscription Confirm Remove. The Medtronic Model Single-Chamber Temporary Pacemaker is medtronic single chamber pacemaker 5348 to be used in conjunction datingsites voor rijke mannen a cardiac pacing lead system for temporary single chamber pacing in a clinical environment by trained personnel. MR unsafe - The temporary pacemaker is MR unsafe. Don't have an account?