Root elevator - Helmut Zepf (17.100.35) - Delynov

What is the Helmut Zepf root elevator (17.100.35)?

The Helmut Zepf root elevator, reference 17.100.35, is a specific manual instrument intended for oral surgery. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is designed in high-quality medical stainless steel. Its structure is engineered to meet the requirements of practitioners during root luxation phases. As a Class I instrument, it complies with the rigorous manufacturing standards imposed on non-invasive or temporary-use invasive medical devices. This equipment is delivered non-sterile by the manufacturer and requires strict preparation before any clinical intervention.

What are the clinical indications for this instrument?

This dental root elevator is indicated for exodontia procedures requiring mechanical separation between the root and the socket. It is primarily used by dental surgeons and implantologists to luxate roots, extract residual fragments, or prepare a socket before implant placement. Its role is crucial for mobilizing the tooth by exerting controlled pressure on the desmodontium. The use of this Helmut Zepf instrument is strictly reserved for qualified healthcare professionals, ensuring handling in accordance with current clinical protocols in oral surgery.

What are the technical characteristics of the 17.100.35 elevator?

The root elevator referenced 17.100.35 is distinguished by its medical stainless steel design, a material chosen for its resistance to repeated sterilization cycles and its biocompatibility. Although specific dimensions are not detailed, its geometry is adapted to the root anatomy to allow optimal support. The manufacturer Helmut Zepf Medizintechnik GmbH emphasizes that the product design and materials used do not allow for a defined maximum limit of reprocessing cycles, as long as the instrument does not show visible damage such as cracks, breaks, or defects on the active parts.

What are the contraindications for the use of this elevator?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals, specifically the medical stainless steel used to manufacture the instrument. An allergic reaction may occur upon contact with the patient's tissues. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any use of this manual instrument in the mouth.

What are the maintenance and sterilization precautions?

Like any Class I instrument delivered non-sterile, the root elevator must imperatively be cleaned, disinfected, and sterilized before its first use, as well as after each subsequent use. The complete reprocessing process must be scrupulously followed. Before each intervention, the practitioner must visually inspect the instrument for any signs of wear, corrosion, or structural degradation. It is strictly forbidden to use a damaged product showing cracks or dull cutting edges. Compatibility with other products used simultaneously must also be verified beforehand by the professional.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany, a recognized manufacturer in the field of dental instrumentation. This product is classified as a Class I device according to current regulations. Although specific CE marking is not detailed in the provided sources, the instrument meets safety and performance requirements for manual stainless steel dental instruments. Compliance with cleaning and sterilization protocols is essential to maintain the device's conformity throughout its clinical life, under the responsibility of the healthcare professional.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.