90 Degree RF Suction Coblation Wand For Orthopedics Treatment

90 Degree RF Suction Coblation Wand for Orthopedics Treatment

Overview

A 90 Degree RF Suction Coblation Wand is used for minimally invasive procedures such as synovial membrane debridement and excision in the knee and shoulder joints. The wand uses radiofrequency energy to ablate and remove tissue while minimizing damage to surrounding healthy tissue. The suction component of the wand helps to remove the ablated tissue and fluid from the surgical site, providing better visualization and reducing the risk of complications such as infection.

The synovial membrane is a thin layer of tissue that lines the joints and produces synovial fluid, which helps lubricate and cushion the joint during movement. However, in some cases, the synovial membrane can become inflamed or damaged, leading to pain, swelling, and stiffness. Synovial membrane debridement and excision may be necessary to remove damaged or diseased tissue and improve joint function.

During the procedure, the surgeon inserts the wand through a small incision in the joint and uses it to remove the damaged tissue while minimizing damage to the surrounding healthy tissue. The suction component of the wand helps to remove the ablated tissue and fluid from the surgical site, providing better visualization and reducing the risk of complications such as infection.

Overall, the 90 Degree RF Suction Coblation Wand is a useful tool for performing minimally invasive joint surgeries, allowing for precise tissue removal and improved patient outcomes.

Specification

Applications

Synovial membrane debridement and excision for knee and shoulder

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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