123mm Radiofrequency Coblation Wand Lumbar Lateral Target Ablation Tip

Radiofequency Coblation Wand Lumbar Lateral Target Ablation Tip

Overview

Using coblation wand to perform an ablation in the spine.

The procedure involves first inserting a puncture needle into the hard spinal membrane more than 2mm and then adding 3-5 drops of physiological saline. The operator then inserts a back probe into the needle sheath to observe the target location.

After this, the operator sets a one-second test power level, and immediately steps on the blue pedal to activate the device. If there are no adverse reactions, the operator can reset the device to adjust the ablation power and time, or they can continuously activate it for 1 second to complete the ablation.

The coblation wand uses a process called coblation, which involves using a high-frequency electrical current to ionize a saline solution and create a plasma field. This plasma field can then be used to remove or ablate tissue in a controlled and precise manner.

The use of a coblation wand for spinal ablation is a highly specialized medical procedure that requires extensive training and expertise to perform safely and effectively. Patients should always consult with their doctors to determine if this procedure is appropriate for their individual needs, and only seek treatment from qualified medical professionals with the appropriate equipment and expertise.

Specification

Applications

Lumbar lateral target ablation

Precautions for the use of plasma coblation wand in combination with plasma console:

(a) Check the expiration date and package integrity of the disposable coblation wand before use.

(b) The patient should not come into contact with the metal components of grounded equipment, and the use of antistatic plates is recommended.

(c) The disposable coblation wand cable should be kept away from patients and other leads, and temporarily unused probes should be stored away from patients.

(d) If the output is significantly reduced or the equipment fails to function normally, it may indicate poor probe contact or improper use.

(e) Flammable cleaning agents and solvents should be evaporated before using the plasma surgical system equipment, and flammable fluids should be wiped off from the patient's body and cavity.

(f) High-frequency current may interfere with cardiac pacemakers, so the current loop should not pass through the active implantable device.

(g) When installing the disposable coblation wand and powering on the equipment, avoid contact between the electrode and metal enclosure, and keep physiological monitoring equipment away from the probe as much as possible.

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