Root elevator after GÄRTNER - Helmut Zepf (17.220.01) - Delynov

What is the Helmut Zepf root elevator after GÄRTNER?

The root elevator after GÄRTNER, referenced under code 17.220.01 by Helmut Zepf, is a precision manual instrument intended for oral surgery. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is designed in high-quality medical stainless steel. Its structure is specifically adapted for the handling of root fragments. As a Class I device, it meets the regulatory requirements for non-invasive or transiently invasive surgical instruments. The product is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient to ensure clinical safety.

What are the clinical indications for this instrument?

This instrument is indicated for exodontia and alveolar surgery procedures. More specifically, the elevator after GÄRTNER is used for the luxation and extraction of roots or residual root fragments. Its application is reserved for healthcare professionals qualified in dental surgery and implantology. It allows for intervention on dental structures during simple or complex extraction phases, facilitating the release of the root from its socket. The use of this Helmut Zepf instrument must be preceded by a verification of the integrity of the cutting edge to ensure optimal function during the intervention.

What are the technical characteristics of this elevator?

The Helmut Zepf elevator (reference 17.220.01) features technical characteristics in accordance with German surgical instrumentation standards. It is entirely designed in medical stainless steel, a material chosen for its resistance to repeated sterilization cycles. The design of the instrument after GÄRTNER is optimized for grip and the application of controlled forces during root luxation. Before each use, the practitioner must visually inspect the instrument to detect any damage such as cracks, breaks, or defects on the active parts. Due to its robust design, there is no defined maximum limit of processing cycles, as long as the visual examination confirms the absence of critical wear.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known patient hypersensitivity to metals. As the instrument is composed of medical stainless steel, contact may trigger an allergic reaction or intolerance in sensitive subjects. If a hypersensitivity reaction manifests during the surgical intervention, the procedure must be immediately interrupted and appropriate medical measures must be initiated. It is the responsibility of the practitioner to check the patient's allergic history before any use of this instrument in the mouth.

What are the maintenance and reprocessing precautions?

Like any reusable Class I surgical instrument, this Helmut Zepf elevator requires a rigorous reprocessing protocol. The products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use. After each surgical act, the instrument must follow a complete cleaning and sterilization cycle. The manufacturer emphasizes the importance of verifying compatibility with other cleaning and disinfection products used. Any instrument showing visible signs of wear, corrosion, or damaged cutting edges must be immediately removed from service to avoid any risk of intraoperative complication.

Who is the manufacturer and what standards are respected?

The root elevator after GÄRTNER is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with strict quality standards for the production of manual dental instruments. The device is classified as Class I according to current regulations. Traceability and compliance are ensured by the manufacturer for this medical stainless steel instrument. As a Class Ir medical device (according to technical marking), it is subject to rigorous control processes guaranteeing its safety of use in a professional setting by trained dental surgeons or implantologists.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.