Elevator Hourrigan Number 12H with Handle Number 510 Striated - Hu-Friedy - Delynov

What is the Hu-Friedy Hourrigan #12H elevator?

The Hourrigan #12H elevator is a high-precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is distinguished by its robust structure adapted to the constraints of oral surgery. It is equipped with a serrated #510 handle, designed to optimize grip during forceful maneuvers. As a Hu-Friedy brand instrument, this elevator benefits from the expertise of a recognized manufacturer in the dental sector. Its design aims to meet the needs of practitioners seeking a reliable tool for the initial stages of dental avulsion, ensuring efficient transmission of force to the active part of the instrument.

What are the clinical indications for this instrument?

This surgical extraction instrument is primarily indicated for the luxation of teeth and roots prior to their final removal. The hourrigan elevator is used in oral surgery to insert into the periodontal space to widen the socket and break ligament attachments. Its use is essential in cases of simple or complex extractions, allowing for the mobilization of the dental element with great precision. The specific design of the #12H model allows access to targeted areas, thereby facilitating the work of the dental surgeon during exodontia protocols. It is a fundamental tool for preparing the socket before the intervention of forceps.

What are the technical characteristics of the serrated #510 handle?

The serrated dental elevator features a #510 type handle, a specific technical reference at Hu-Friedy. The main characteristic of this handle lies in its serrated surface, which ensures maximum stability, even in wet environments or when wearing surgical gloves. This texture helps prevent accidental slippage, thus providing increased safety for both the patient and the practitioner. The geometry of the handle is designed to provide effective leverage while maintaining the tactile sensitivity necessary to evaluate bone resistance. This technical design reflects Hu-Friedy's commitment to providing ergonomic instruments for the daily practice of implantology and oral surgery.

What are the contraindications for the use of this elevator?

In accordance with information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. General clinical contraindications apply, notably use on unsuitable anatomical structures or for functions other than dental elevation and luxation. It is imperative not to use the instrument if it shows signs of wear or deformation, as this could compromise the safety of the surgical procedure. Practitioners must refer to the instructions for use and current clinical protocols to ensure the suitability of the instrument for the patient's specific clinical situation.

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

As a reusable surgical instrument, the Hourrigan elevator requires a rigorous sterilization and cleaning protocol after each use. Although composition specificities are not detailed here, Class I Hu-Friedy instruments must be processed according to the manufacturer's instructions to maintain their structural integrity. Precautions include a pre-disinfectant cleaning, followed by appropriate sterilization in an autoclave. It is crucial to check the condition of the #510 handle serrations and the active part before each intervention. Proper maintenance not only guarantees the hygiene essential to the operating room but also extends the operational life of this surgical extraction instrument.

Who is the manufacturer and what standards are respected?

The Hourrigan #12H elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This medical device belongs to Class I according to current regulations. As a Hu-Friedy product, it is designed according to rigorous manufacturing standards to meet the requirements of healthcare professionals. The manufacturer emphasizes that this instrument is exclusively reserved for professional use. Users are invited to read the instructions carefully before use to comply with safety guidelines and warnings. This Class I regulatory status confirms that the instrument meets the essential safety and performance criteria defined for medical devices in this category.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.