Special Elevator Fig-62 4mm Light - Helmut Zepf (17.101.62) - Delynov

What is the Helmut Zepf Fig-62 4 mm special elevator?

The Fig-62 special elevator, referenced under code 17.101.62, is a manual instrument designed by Helmut Zepf Medizintechnik GmbH. This device is characterized by a 4 mm working part, specifically sized for exodontia procedures. Manufactured from medical stainless steel, this instrument is intended for the manipulation of dental structures during luxation phases. As a Class I device, it meets the regulatory requirements for reusable non-invasive or short-term invasive surgical instruments. Its lightweight structure allows for a grip adapted to the requirements of daily oral surgery, while maintaining the necessary rigidity for leverage maneuvers.

What are the clinical indications for this instrument?

This 4mm dental elevator is primarily indicated for the luxation of teeth and roots prior to forceps extraction. In oral and implant surgery, it is used to break the periodontal ligament fibers and widen the socket, thus facilitating the removal of the dental element. The 4mm elevator is particularly useful for mobilizing fractured roots or firmly anchored teeth. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, acting in a sterile clinical environment to prevent infection risks.

What are the technical characteristics of this elevator?

The Helmut Zepf instrument (reference 17.101.62) features a 4 mm tip width, optimized to fit into the periodontal space. Its monobloc design in medical stainless steel ensures direct force transmission during rotation or leverage movements. The manufacturer, Helmut Zepf Medizintechnik GmbH, delivers this product non-sterile, which requires a complete processing cycle before the first use. The design of the instrument does not define a maximum limit of processing cycles, as the service life depends on actual physical wear, such as the appearance of cracks or defects on the edges, which must be systematically checked.

What are the contraindications for the use of this elevator?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with an allergic patient can trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of the instrument is prohibited if visible damage is detected, such as breaks, cracks, or pronounced wear of the cutting edges, to guarantee patient safety and the effectiveness of the surgical gesture.

What are the maintenance and sterilization precautions?

Like any reusable Class I instrument, this elevator must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. Helmut Zepf specifies that the products are delivered non-sterile. The reprocessing process must include thorough cleaning to remove all organic debris before the sterilization phase. It is crucial to check the integrity of the instrument before each intervention: any sign of physical degradation (cracks, defects on the 4 mm tip) renders the instrument unfit for use. Compatibility with other cleaning and disinfection products must also be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to the current regulations (MDR). Compliance with Helmut Zepf manufacturing standards guarantees the use of high-quality medical stainless steel. Although specific CE marking is not detailed in the source data, the instrument follows the safety and performance protocols applicable to manual dental instruments. Compliance with the instructions for use and safety provided by the manufacturer is imperative to maintain the device's conformity during its life cycle in the dental practice.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.