Root elevator - Helmut Zepf (17.303.00) - Delynov

What is the Helmut Zepf root elevator (17.303.00)?

The Helmut Zepf root elevator, referenced under code 17.303.00, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed for oral surgery, this tool is crafted from high-quality medical stainless steel, ensuring resistance adapted to mechanical stresses during dental extractions. As a Class I device, it meets regulatory requirements for non-invasive or invasive instruments for temporary use. Its structure is optimized to allow rigorous handling by the practitioner, facilitating access to alveolar areas for root mobilization.

What are the clinical indications for this instrument?

The intended use of this Helmut Zepf instrument is as a manual dental instrument intended for exodontia procedures. It is specifically indicated for the luxation of dental roots, the elevation of root fragments, and the separation of the periodontal ligament from the alveolar wall. Its clinical application extends from simple extraction to implant surgery requiring careful alveolar preparation. The instrument is reserved exclusively for qualified healthcare professionals, ensuring application in accordance with current surgical protocols in odontology and maxillofacial surgery.

What are the technical characteristics of the device?

This Helmut Zepf elevator, bearing technical reference 17.303.00, is characterized by its manufacture in medical stainless steel. Although delivered non-sterile, it is designed to withstand repeated cycles of cleaning, disinfection, and sterilization without major alteration of its mechanical properties. The manufacturer specifies that due to the robust design and materials used, there is no defined maximum limit for processing cycles, subject to prior visual inspection. Every practitioner must verify the absence of visible damage such as cracks, breaks, or defects on the cutting edges before any intervention.

What are the contraindications for the use of this elevator?

The main medical contraindication documented by Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Contact of the medical stainless steel instrument with an allergic patient can trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to validate the patient's anamnesis regarding allergies to metallic components before any use of this surgical instrument in the mouth.

What are the maintenance and reprocessing precautions?

Helmut Zepf products are delivered non-sterile and require a strict protocol before the first use and between each patient. All instruments must be fully cleaned, disinfected, and sterilized. It is crucial to inspect the elevator to detect any visible wear, particularly on the active parts. The use of a damaged instrument, presenting cracks or blunt edges, is prohibited to ensure patient safety. Compatibility with other cleaning and sterilization products must also be verified beforehand to preserve the integrity of the medical stainless steel.

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 certain reprocessing nomenclatures). The manufacturer respects the manufacturing standards for manual dental instruments in stainless steel. As a Class I device, it follows the safety and performance requirements defined by European regulations on medical devices. Traceability is ensured by the reference 17.303.00, allowing precise identification within the brand's range of oral surgery instruments.

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