Labanca #3 periosteal elevator #41 handle

What is the Labanca #3 periosteal elevator handle #41 from the brand Marque?

The Labanca #3 periosteal elevator, equipped with the #41 handle, is a specialized surgical instrument belonging to the INSTRU category. Developed by the manufacturer Hu-Friedy, this device is designed to meet the requirements of oral surgery procedures. The brand Marque offers this precision tool to facilitate delicate interventions requiring rigorous tissue manipulation. As a Class I instrument, it is specifically developed for healthcare professionals. Its ergonomic design via the #41 handle allows for optimal grip during the elevation phases, thus ensuring increased clinical efficiency during surgical acts in dental offices or hospital settings.

What are the clinical indications for this device?

The Labanca #3 periosteal elevator from the brand Marque is indicated for oral surgery, implantology, and periodontology procedures. Its use is strictly reserved for qualified healthcare professionals. It is primarily used to lift and separate the periosteum from the bone, thus allowing clear exposure of the surgical site. This device is essential for the creation of full-thickness flaps. According to the indications from the manufacturer Hu-Friedy, this instrument must be used in accordance with current surgical protocols. Its role is decisive in ensuring adequate visibility and secure access to anatomical structures during critical phases of the surgical procedure.

What are the technical characteristics of this instrument?

The Labanca #3 periosteal elevator is distinguished by the integration of the #41 handle, offering ergonomics adapted to the needs of dental surgeons. This device in the INSTRU category is classified as a Class I instrument. Manufactured by Hu-Friedy in Chicago, it benefits from the technical expertise of a world leader in dental instrumentation. Although specific details on materials are not provided, its structure is designed to withstand the stresses of tissue elevation procedures. The brand Marque ensures the distribution of a reliable tool, whose technical configuration allows for the precision of movement indispensable during the manipulation of soft and hard tissues in oral surgery.

What are the contraindications for the use of the Labanca #3 periosteal elevator?

The use of the Labanca #3 periosteal elevator is contraindicated for any person who is not a qualified healthcare professional. Specific contraindications related to the patient's clinical status must be evaluated by the practitioner before any intervention. It is imperative not to use the instrument if it shows signs of deterioration or if sterility conditions are not guaranteed. The manufacturer Hu-Friedy emphasizes the importance of respecting the intended use to avoid any risk of unintentional tissue injury. A careful reading of the instructions for use is mandatory before any clinical implementation to ensure patient safety and device integrity.

What are the precautions for use and maintenance for this non-resorbable device?

As a reusable and non-resorbable surgical instrument, the Labanca #3 periosteal elevator requires rigorous maintenance protocols. Precautions include thorough cleaning and systematic sterilization between each patient, in accordance with the warnings from the manufacturer Hu-Friedy. Healthcare professionals must inspect the instrument before each use to ensure the absence of corrosion or deformation. Careful handling is required to preserve the active edges of the elevator. Compliance with the recommended sterilization cycles is crucial to maintain the performance of the Class I instrument and ensure the longevity of the equipment within daily surgical practice.

Who is the manufacturer and what standards are met by this product?

The Labanca #3 periosteal elevator handle #41 is manufactured by Hu-Friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, meeting the regulatory requirements for surgical instruments in this category. The manufacturer dictates that the use of this instrument be strictly reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, the product follows strict directives relating to medical devices of its class. It is essential to carefully read the instructions for use provided by the manufacturer to ensure application in accordance with current safety and clinical efficacy standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.