Warwick-James Elevator Handle Number 504 Left - Hu-Friedy - Delynov

What is the Warwick-James elevator handle #504 left?

The Warwick-James elevator handle #504 left is an oral surgery instrument manufactured by Hu-Friedy. It consists of a laterally oriented working part and an ergonomic #504 type handle. This device is designed to apply precise leverage forces during extraction procedures. As a manual instrument, it is used by the surgeon to break ligament fibers and mobilize the tooth or root before its final removal. The manufacturing quality of Hu-Friedy Mfg. Co., LLC guarantees a tool adapted to the requirements of dental and implant surgery operating rooms.

What are the clinical indications?

The use of this elevator is indicated in simple or complex dental extraction protocols. It is primarily used during the luxation phase, allowing for the creation of space between the alveolar bone and the root. This Warwick-James left model is particularly useful for reaching posterior sectors or specific angulations where a straight instrument would not allow for optimal support. It can be used in conjunction with a syndesmotome to release the epithelial-connective attachment before the actual elevation, thus facilitating avulsion while preserving the integrity of the surrounding bone plates.

What are the technical characteristics?

This instrument is distinguished by its specific Warwick-James design with a left-oriented curvature. The #504 handle offers a stable grip for the practitioner, allowing for rigorous control of the applied force. Manufactured by Hu-Friedy, this elevator meets Class I standards for medical devices. Its geometry is designed to effectively insert into the periodontal space. Although exact materials are not specified in the source data, the reputation of the manufacturer Hu-Friedy ensures mechanical strength adapted to the torsional stresses encountered during root elevation maneuvers.

What are the contraindications for use?

Specific contraindications for the use of this instrument are not exhaustively listed in the technical documentation provided, beyond the manufacturer's general warnings. From a clinical perspective, its use should be avoided if visual access is insufficient or if the supporting bone structure is too fragile to support the lever's fulcrum. As indicated by Hu-Friedy Mfg. Co., LLC, use is strictly reserved for qualified healthcare professionals. It is the practitioner's responsibility to evaluate the relevance of the instrument based on the patient's anatomy and the condition of the periodontal tissues.

What are the precautions for use and maintenance?

As a Class I device, this elevator is intended for professional use. Before any intervention, it is imperative to carefully read the instructions provided by the manufacturer Hu-Friedy. Although sterilization details are not provided here, this type of surgical instrument requires rigorous cleaning and sterilization between each patient in accordance with hospital or office protocols. The practitioner must take care not to apply excessive force that could damage the instrument or cause an alveolar fracture. A visual inspection of the working end is recommended before each use to ensure the absence of deformation.

Who is the manufacturer and what standards are met?

The elevator is manufactured by Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This medical device is listed as Class I according to current regulations. The manufacturer emphasizes that the use of this instrument is exclusively reserved for healthcare professionals trained in oral surgery techniques. Although CE marking is not explicitly mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures conformity with safety requirements for manual surgical instruments. Users should refer to the instructions and warnings provided by the Chicago facility for compliant use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.