Elevating Root Elevator according to GÄRTNER - Helmut Zepf (17.013.00) - Delynov

What is the GÄRTNER root elevator - Helmut Zepf?

The GÄRTNER root elevator, referenced under code 17.013.00, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed for alveolar-dental surgery, this instrument is made of high-quality medical stainless steel to ensure optimal resistance during applied leverage forces. It consists of an ergonomic handle and a specific working part adapted to the root anatomy. As a Class I device, it meets the safety requirements for temporary-use invasive instruments. This particular model is recognized in clinical practice for its effectiveness during the initial luxation phase, allowing the root to be separated from its alveolar attachment.

What are the clinical indications for this instrument?

The dental Gärtner elevator is primarily indicated for the extraction of roots and root debris. In oral surgery and implantology, it is used before implant placement to perform extractions that are as minimally invasive as possible for the surrounding alveolar bone. The root extraction elevator is used to insert into the periodontal space, applying controlled pressure to break the alveolar-dental ligament. It is particularly useful for roots fractured below the gingival level or for mobilizing single teeth before using forceps. Its use is strictly reserved for qualified healthcare professionals mastering dental surgery techniques.

What are the technical characteristics of the 17.013.00 elevator?

This Helmut Zepf instrument is distinguished by its technical reference 17.013.00. Although exact dimensions are not specified, its design is based on Gärtner root elevator standards, offering a working tip adapted to restricted spaces. Manufactured from medical stainless steel, it exhibits high resistance to corrosion and repeated mechanical stress. The device is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and requires a complete reprocessing cycle before each use. The instrument's design does not define a maximum limit for treatment cycles, as this depends on visible wear, potential damage, or the appearance of cracks on the cutting edges.

What are the contraindications for the use of this elevator?

The main medical contraindication mentioned by the manufacturer concerns metal intolerance. If a patient has a known sensitivity or allergy to medical stainless steel components, the use of this instrument may trigger a hypersensitivity reaction. In such a case, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to ensure patient safety and the effectiveness of the surgical procedure.

What are the maintenance and sterilization precautions?

Like any Class I instrument intended for surgery, this fine root elevator must imperatively be cleaned, disinfected, and sterilized before its first use and after each subsequent use. The reprocessing process must be complete to guarantee asepsis. Before each use, the practitioner must carefully inspect the instrument to detect any signs of wear or structural damage. Due to the materials used, there is no predefined maximum number of sterilization cycles, but compatibility with other cleaning and disinfection products must be verified beforehand. Rigorous maintenance is essential to maintain the mechanical properties of the medical stainless steel.

Who is the manufacturer and what standards are respected?

The elevator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer imposes strict cleaning and sterilization protocols in accordance with health safety standards for manual instruments. Helmut Zepf products are designed for professional use in clinical and hospital environments. Compliance with the instructions for use and safety provided by Helmut Zepf Medizintechnik GmbH is imperative to ensure the longevity of the instrument and the safety of care during root extraction interventions.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.