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Kirsch sinus lift elevator small, 120°/120° angulation - Helmut Zepf (41.868.04S) - Delynov

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The Élévateur sinusien de Kirsch "petit", angulation 120°/120° - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.868.04S.
  • Reserved for healthcare professionals. Read instructions carefully before use.

128.35 € 128.35 EUR 128.35 € Tax Included

128.35 € Tax Included

(0.00 € / Units)
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Instrument

What is the Helmut Zepf small Kirsch sinus elevator?

The Kirsch sinus elevator, referenced under code 41.868.04S, is a specialized manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This model is distinguished by its size classified as "small" and its rigid metallic structure adapted for precision instrumentation. It features a double angulation of 120°/120°, allowing for ergonomic handling during critical phases of sinus surgery. As an instrument in the INSTRU category, it is intended for use by healthcare professionals trained in oral surgery techniques to manipulate soft tissues within a bony cavity.

What are the clinical indications for this instrument?

This dental surgery sinus elevator is primarily indicated for sinus membrane elevation (sinus lift) via a lateral approach. Its use occurs after the creation of the bony window, where it serves to carefully detach the Schneiderian membrane from the internal walls of the maxillary sinus. Its "small" design makes it particularly useful in clinical cases where working space is limited or when the sinus morphology requires a thinner instrument to avoid any perforation. It is employed in vertical bone reconstruction protocols aimed at increasing the volume available for subsequent dental implant placement.

What are the technical characteristics of this elevator?

The Kirsch elevator 41.868.04S presents precise geometric specifications with an angulation of 120°/120°. This double inclination is designed to facilitate the passage of the instrument through the lateral window while maintaining an active tip parallel or adapted to the curvature of the sinus wall. The "small" designation indicates a working part with reduced dimensions compared to standard models in the Helmut Zepf range, thus offering better visibility and increased control when detaching the membrane edges. Its manufacture by Helmut Zepf Medizintechnik GmbH guarantees rigorous adjustment of the angles to meet the requirements of modern implantology.

What are the contraindications for the use of this instrument?

Contraindications for the use of the Kirsch sinus elevator are primarily related to the general contraindications of sinus graft surgery. These include acute sinusitis, local tumor pathologies, or active infections in the maxillary area. Technically, the use of this instrument is discouraged if the Schneiderian membrane shows excessive cicatricial adhesions or if the patient's anatomy does not allow for safe passage of the 120° angulation. As with any metallic instrument, it is appropriate to check for the absence of known allergies to the alloy components before any intervention.

What are the maintenance and handling precautions?

As a reusable surgical instrument, the Helmut Zepf elevator must strictly follow a complete cycle of decontamination, cleaning, and sterilization between each patient. It is recommended to use cleaning solutions that do not alter the properties of the steel and to proceed with autoclave sterilization according to the cycles validated by the manufacturer. During the intervention, the practitioner must ensure not to exert excessive pressure on the membrane to limit the risk of tearing. A visual inspection of the surface condition and the integrity of the 120°/120° angles is necessary before each use to guarantee clinical safety.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-quality dental and surgical instrumentation. Although specific regulatory class or CE marking data are not explicitly detailed in the current technical sheet, Helmut Zepf products are designed to meet the requirements for professional medical devices. The practitioner is invited to systematically refer to the instructions for use and labeling provided with the 41.868.04S instrument to confirm current certifications and reprocessing protocols compliant with health safety standards.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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