Elevator Warwick-James Handle Number 506 Straight - Hu-Friedy - Delynov

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

The Warwick-James elevator #504 handle straight is a high-precision extraction instrument manufactured by Hu-Friedy. This device is specifically designed for oral surgery interventions requiring effective luxation of teeth or roots. Its structure includes an ergonomic #504 type handle providing a stable grip for the practitioner, extended by a straight active part. As an instrument in the INSTRU category, it meets the quality requirements of a recognized manufacturer such as Hu-Friedy Mfg. Co., LLC. This device is intended for strict professional use in dental practices or hospital environments for dental and implant surgery procedures.

What are the clinical indications for this instrument?

The warwick-james elevator is primarily indicated for the luxation of teeth before the use of forceps or for the extraction of fractured roots. In oral surgery, its role is crucial for breaking the fibers of the periodontal ligament and widening the socket. This straight model is particularly suitable for clinical sectors where direct access is possible, allowing for effective leverage. It can also be used as a warwick-james syndesmotome in certain phases of syndesmotomy to detach the epithelial attachment before the extraction itself. Its use is reserved for healthcare professionals trained in surgical techniques for tooth luxation and avulsion.

What are the technical characteristics of the #504 handle?

The Hu-Friedy Warwick-James straight elevator features a specific handle referenced under the number #504. This handle is designed to offer an optimal balance between the weight of the instrument and the leverage force required during extractions. The technical design by Hu-Friedy ensures precise force transmission to the straight active tip, minimizing the effort required by the surgeon while maximizing the efficiency of the movement. Although the exact material composition is not specified in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC guarantees an instrument meeting the rigorous standards of Class I for reusable medical devices.

What are the contraindications for the use of this elevator?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than those related to standard tooth extraction protocols. However, the use of the warwick james syndesmotome is contraindicated in patients with uncontrolled systemic pathologies that could compromise healing or increase the risk of hemorrhage, unless otherwise advised by the surgeon. It is imperative to carefully read the instructions for use and follow the warnings from the manufacturer located in Chicago, USA, before any clinical intervention.

What are the maintenance precautions for this non-resorbable instrument?

As a Class I reusable surgical instrument, the Warwick-James straight elevator requires a rigorous sterilization and cleaning protocol between each patient. Although cleaning specificities are not detailed here, Hu-Friedy devices must be processed according to the manufacturer's instructions to maintain their structural integrity. The condition of the active part should be checked before each use to ensure the absence of deformation. Compliance with standard sterilization cycles is essential to guarantee aseptic safety during oral surgery procedures and to avoid any cross-contamination in the dental practice.

Who is the manufacturer and what standards are met?

The Warwick-James elevator #504 handle straight is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device belongs to Class I according to current regulations. As a product distributed by Delynov, it complies with safety requirements for surgical instruments reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, the Class I status confirms its regulatory registration for use in dental surgery. Practitioners must systematically refer to the instructions and warnings provided by Hu-Friedy for compliant use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.