Elevator Apex Number 302 with Handle Number 510 - Hu-Friedy - Delynov

What is the #302 apex elevator with #510 handle?

The #302 apex elevator with #510 handle is a high-precision manual instrument manufactured by Hu-Friedy. This device is specifically designed for oral surgery interventions requiring delicate manipulation of root structures. Its structure consists of a refined working part, the #302 apex, mounted on an ergonomic handle reference #510, offering a grip adapted to the requirements of practitioners. As an instrument in the INSTRU category, it meets the rigorous manufacturing standards of Hu-Friedy Mfg. Co., LLC, ensuring constant reliability during daily clinical procedures in dental offices or hospital environments.

What are the clinical indications for this instrument?

This dental apex elevator is primarily indicated for the luxation of roots and root debris. Its use is recommended during dental extractions where access is restricted or when the root is fractured below the alveolar level. In implant or oral surgery, it allows for tooth mobilization by exerting controlled pressure, thereby facilitating avulsion while best preserving the integrity of the surrounding alveolar bone. The instrument is exclusively reserved for qualified healthcare professionals trained in extraction and dental surgery techniques, in accordance with the usage guidelines from the manufacturer Hu-Friedy located in Chicago.

What are the technical characteristics of the elevator?

The #302 apex elevator is distinguished by its technical configuration combining a specific active tip and a #510 type handle. Although the precise materials are not specified in the provided technical documentation, the instrument benefits from Hu-Friedy's expertise in surgical engineering. The design of the #302 apex is optimized to insert effectively into the socket, while the #510 handle ensures adequate force transmission without compromising the surgeon's tactile sensitivity. This device is classified as a Class I instrument, highlighting its compliance with regulatory requirements for non-invasive or temporary-use invasive medical devices.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for healthcare professionals. General contraindications include use by unqualified personnel or for procedures not in accordance with the instrument's intended purpose. It is imperative to consult the instructions for use before any intervention to identify any specific restrictions related to the patient's clinical condition or underlying pathologies that could compromise the success of the surgical act. Compliance with sterilization and maintenance protocols is also essential to avoid any risk of cross-contamination or technical failure.

What are the precautions for use and maintenance?

Like any Class I surgical instrument, the apex elevator must be handled with care to maintain its performance. Before each use, the practitioner must visually inspect the instrument to ensure the absence of damage or excessive wear on the #302 active part or the #510 handle. Although the resorption process does not apply to this non-resorbable metallic instrument, precautions mainly concern cleaning, disinfection, and systematic sterilization between each patient. It is crucial to carefully follow the instructions for use provided by Hu-Friedy to guarantee the longevity of the instrument and the safety of the care provided.

Who is the manufacturer and what standards are respected?

The #302 apex elevator is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized company located at 3232 N. Rockwell St. in Chicago, USA. This medical device belongs to Class I according to current regulations. The manufacturer emphasizes that this instrument is exclusively reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, the Class I regulatory classification attests that the product meets the safety and performance requirements defined for this category of medical devices. Users are invited to read the instructions carefully before any clinical implementation.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.