Root elevator according to GÄRTNER - Helmut Zepf (17.013.02) - Delynov

What is the GÄRTNER root elevator?

The GÄRTNER root elevator, referenced under code 17.013.02 by Helmut Zepf, is a precision manual instrument used in oral surgery. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device is designed to withstand mechanical stress during avulsion procedures. Its structure is specifically adapted to be inserted between the socket and the dental root. As a Class I instrument, it meets the quality requirements for non-invasive or temporary invasive medical devices. It is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and after each intervention.

What are the clinical indications for this instrument?

This extraction surgery instrument is primarily indicated for the luxation of roots and radicular fragments. The gärtner surgery elevator is used by practitioners to separate the tooth from its alveolar attachment by applying controlled pressure. It is particularly useful in cases of difficult extractions where simple forceps are not sufficient to mobilize the dental structure. Its application allows for the preparation of the site for a less traumatic extraction of the surrounding tissues. Use of this curved root elevator is reserved exclusively for qualified healthcare professionals mastering dental and implant surgery techniques.

What are the technical characteristics of the 17.013.02 elevator?

The GÄRTNER root elevator is distinguished by its technical reference 17.013.02. Designed by the manufacturer Helmut Zepf, it is crafted from high-quality medical stainless steel to ensure optimal biocompatibility, provided there is no metal allergy. Its ergonomic design allows for efficient force transmission during luxation. In accordance with the manufacturer's guidelines, the instrument does not have a defined maximum limit of processing cycles, as its lifespan depends on actual wear and the absence of visible damage such as cracks or defects on the edges. Compatibility with other instruments must be verified by the practitioner before the surgical act.

What are the contraindications for using this elevator?

The main medical contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, particularly to the medical stainless steel used for the manufacture of the instrument. If a hypersensitivity reaction is triggered in the patient upon contact, the procedure must be immediately stopped and necessary clinical measures must be taken. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage, cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the surgical gesture.

What are the maintenance and reprocessing precautions?

Like any reusable Class I instrument, the curved root elevator must follow a rigorous reprocessing cycle. Helmut Zepf products are delivered non-sterile. It is imperative to carry out complete cleaning, disinfection, and sterilization before the first use and between each patient. The manufacturer emphasizes the importance of checking the condition of the instrument before each use to detect any trace of wear or corrosion. Due to its robust stainless steel design, there is no predetermined number of cycles, but the physical integrity of the tool must be visually validated by the healthcare professional before any intervention in the mouth.

Who is the manufacturer and what standards are respected?

The GÄRTNER root elevator is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to reprocessing specifications) in accordance with current medical device regulations. The manufacturer respects manufacturing standards for manual dental instruments in medical stainless steel. Each product is identified by a precise reference, here the code 17.013.02, ensuring the traceability of the device. Compliance with the cleaning and sterilization instructions recommended by Helmut Zepf is essential to guarantee the conformity and safety of the instrument during its clinical use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.