Root Elevator - Helmut Zepf (17.010.03) - Delynov

What is the Helmut Zepf 17.010.03 root elevator?

The Helmut Zepf root elevator, reference 17.010.03, is a specialized manual instrument for oral surgery. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device is designed to offer structural resistance adapted to mechanical stresses during extractions. Its metallic composition ensures compatibility with thermal and chemical reprocessing protocols in the dental office. As an instrument in the INSTRU category, it meets the rigorous manufacturing requirements of the German manufacturer to guarantee precise handling during routine or complex interventions.

What are the clinical indications for this instrument?

This instrument is indicated for the elevation and luxation of dental roots. In clinical practice, it is used by the surgeon to separate the tooth from its socket by acting on the periodontal ligament, thus functioning as a manual syndesmotome. It is particularly requested during extractions of fractured or impacted roots where prior mobilization is necessary before using forceps. Its application is strictly reserved for qualified healthcare professionals within the framework of oral surgery, implantology, or periodontology procedures requiring precise root access.

What are the technical characteristics of the 17.010.03 elevator?

The Helmut Zepf 17.010.03 elevator is characterized by its manufacture in high-quality medical stainless steel. It is a non-sterile instrument upon delivery, requiring a complete cycle of cleaning, disinfection, and sterilization before the first use and between each patient. The product design and materials used do not allow for a defined maximum limit of processing cycles, although the user must inspect the instrument for any visible damage such as cracks, breaks, or wear of the cutting edges before any intervention.

What are the contraindications for the use of this device?

The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Contact with medical stainless steel can trigger an allergic reaction in certain sensitive patients. If such a hypersensitivity reaction occurs during the surgical act, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before using this manual instrument in the mouth.

What are the maintenance and reprocessing precautions?

Like any reusable Helmut Zepf instrument, this elevator must undergo a strict reprocessing protocol. Before each use, the instrument must be cleaned, disinfected, and sterilized to prevent risks of cross-contamination. It is imperative to check for the absence of defects on the active parts, as the use of damaged or worn products is prohibited. Due to its non-resorbable nature and its temporary intraoperative use, maintenance focuses on the integrity of the cutting edges and the absence of corrosion to maintain the performance of the instrument during luxation maneuvers.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). It complies with the brand's quality standards for manual instruments. The manufacturer states that compatibility with other products must be verified beforehand. As a Class I device, it is intended exclusively for professional use by trained practitioners, thus guaranteeing application in accordance with safety data and current clinical protocols.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.