Special Elevator 2 Millimeters Figure 60 - Helmut Zepf (17.101.60)

What is the figure 60 2 millimeter special elevator?

The figure 60 2 millimeter special elevator, referenced under code 17.101.60 by Helmut Zepf, is a manual instrument designed for exodontic surgery. This small dental elevator is distinguished by a narrow 2mm working part, adapted to restricted spaces. Manufactured from medical stainless steel, it features a rigid structure allowing for the application of leverage forces necessary for root mobilization. As a Helmut Zepf brand device, it meets the quality requirements of German surgical instrumentation for repeated use after reprocessing.

What are the clinical indications?

This 2mm dental elevator is primarily indicated for the luxation and extraction of roots or dental fragments. Its thin profile is particularly useful during atraumatic extraction procedures where preservation of the alveolar bone plate is critical, especially in view of immediate implantation. It allows access to fractured or deeply anchored roots by inserting into the periodontal space. The use of this 2mm elevator is reserved for qualified healthcare professionals practicing oral surgery and implantology.

What are the technical characteristics?

The Helmut Zepf elevator (reference 17.101.60) features a figure 60 type active tip with a width of 2 millimeters. Its medical stainless steel design ensures the mechanical resistance essential for torsion and leverage stresses during exodontia. This device is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. The instrument design does not define a maximum limit of treatment cycles, subject to a prior visual inspection.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Medizintechnik GmbH concerns patients with a known intolerance or hypersensitivity to metals, specifically to medical stainless steel. If a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Additionally, the use of the instrument is contraindicated if visible damage such as cracks, breaks, or defects on the cutting edges are noted during the preoperative inspection.

What are the maintenance and safety precautions?

Like any non-absorbable and reusable instrument, this thin dental elevator must be cleaned, disinfected, and sterilized before each use. It is imperative to check the condition of the instrument before any handling to detect possible wear or damage. The use of damaged products is strictly prohibited. Reprocessing must follow standard hospital or dental office sterilization protocols. Due to its metallic composition, compatibility with other cleaning products and sterilization cycles must be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to the reference text). It is designed to meet the requirements of healthcare professionals regarding manual dental instrumentation. The manufacturer specifies that the product must be handled exclusively by qualified personnel. Traceability and compliance with safety standards are ensured by following the cleaning and sterilization protocols defined by the manufacturer for medical stainless steel.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.