Root Elevator - Helmut Zepf (17.100.09) - Delynov

What is the Helmut Zepf root elevator (17.100.09)?

The Helmut Zepf root elevator, referenced under code 17.100.09, is a manual instrument designed specifically for oral surgery. Manufactured from medical stainless steel, this device is intended for the luxation of dental structures. As a Class I instrument, it meets the quality requirements for non-invasive or invasive medical devices for temporary use. Its robust structure allows for controlled force transmission during extraction maneuvers. This product is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and requires a complete preparation cycle before its first use in the practice.

What are the clinical indications for this instrument?

This dental elevator is indicated for the extraction of roots and teeth. In clinical practice, it is used by the dental surgeon to separate the root from its socket by severing the periodontal ligament fibers. It is particularly useful in cases of fractured or deeply anchored roots where standard forceps cannot be applied effectively. Its role is to create sufficient mobility to finalize the avulsion. The use of this root extraction instrument is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of this elevator?

The Helmut Zepf elevator (17.100.09) is characterized by its medical stainless steel composition, guaranteeing the mechanical resistance necessary for leverage stresses. Although specific dimensions are not detailed, its design is optimized for manual grip and access to alveolar areas. The manufacturer does not define a maximum limit for processing cycles, as the service life depends on use and maintenance. It is imperative to check for the absence of visible damage, such as cracks or defects on the cutting edges, before each intervention to ensure the effectiveness of the surgical gesture.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance of the patient to metals, specifically to medical stainless steel. An allergic reaction may be triggered upon contact with the instrument. If such a hypersensitivity reaction occurs during the procedure, the intervention must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to validate the patient's anamnesis regarding allergies to metallic components before any use of this Class I instrument.

What are the maintenance and reprocessing precautions?

Like all Helmut Zepf products, this elevator is delivered non-sterile. Safety instructions require that the instrument be cleaned, disinfected, and sterilized before the first use, and then after each subsequent use. The reprocessing process must be complete to prevent any risk of cross-contamination. The practitioner must inspect the instrument for any wear, cracks, or breakage before use. The use of damaged or worn products is prohibited. Due to the materials used, the number of achievable sterilization cycles is not limited by a predefined value, but by the observed physical condition of the steel.

Who is the manufacturer and what standards are respected?

The root elevator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its production processes to meet the requirements of healthcare professionals. Traceability is ensured by technical reference 17.100.09. Compliance with cleaning and sterilization protocols by the end user is essential to maintain the compliance and safety of the device throughout its operational life within the healthcare facility.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.