Special Elevator 3 mm Figure 61 - Helmut Zepf (17.100.61) - Delynov

What is the special elevator 3 mm figure 61?

The special elevator 3 mm figure 61, bearing reference 17.100.61, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This device is designed in medical stainless steel, a standard material for surgical instrumentation ensuring resistance adapted to mechanical stresses during avulsion procedures. As a 3mm dental elevator, it features a working part calibrated to insert effectively into the socket. This product belongs to Class I of medical devices, meeting the regulatory requirements for non-invasive or invasive instruments for temporary use.

What are the clinical indications?

This instrument is indicated for use in oral and implant surgery, primarily during dental extraction phases. Its main role is luxation, which consists of mobilizing the tooth or root by applying controlled pressure to break the periodontal attachments. The use of this Helmut Zepf elevator is particularly relevant for preparing the socket before immediate implant placement or for extracting root debris. It is exclusively reserved for qualified healthcare professionals mastering manual dental surgery techniques.

What are the technical characteristics?

The Helmut Zepf elevator reference 17.100.61 is characterized by a tip width of 3 mm, corresponding to figure 61 of the manufacturer's catalog. Its monobloc structure in medical stainless steel ensures direct transmission of the force applied by the practitioner. The device is delivered non-sterile, which requires a strict processing protocol before the first use and between each patient. The design of the instrument does not define a maximum limit of processing cycles, although natural wear and the condition of the edges must be visually checked before each intervention.

What are the contraindications for use?

The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, specifically to medical stainless steel. In the event of an allergic reaction or hypersensitivity triggered during contact with the instrument, the surgical procedure must be immediately interrupted and necessary clinical measures must be taken. Furthermore, the use of the instrument is prohibited if it shows visible damage such as cracks, breaks, or defects on the cutting edges, in order to avoid any iatrogenic risk.

What are the maintenance and sterilization precautions?

Like any reusable Class I instrument, this elevator must imperatively be cleaned, disinfected, and sterilized before its first commissioning and after each subsequent use. The manufacturer specifies that it is crucial to perform a complete cleaning to remove any biological residue before the sterilization cycle. Practitioners must inspect the instrument for any trace of wear or corrosion. Being delivered non-sterile, compliance with current reprocessing protocols in the dental office is essential to guarantee the aseptic safety of care.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). It respects the manufacturing requirements for manual instrumentation in medical stainless steel. Compatibility with other products and reprocessing cycles must be verified by the healthcare professional. Following the safety instructions from the manufacturer Helmut Zepf is essential to maintain the integrity of the instrument and patient safety during surgical interventions.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.