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Elevator Kirsch Sinus 1 to 25 degrees - Helmut Zepf (41.868.01) - Delynov

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The Élévateur Kirsch Sinus 1 à 25 degrés - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.868.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

120.80 € 120.8 EUR 120.80 € Tax Included

120.80 € Tax Included

(120.80 € / Units)
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Instrument

What is the Helmut Zepf Kirsch Sinus Elevator 1 at 25 degrees?

The Kirsch Sinus Elevator 1 at 25 degrees (reference 41.868.01) is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this instrument belongs to the Class I device category. Its specific structure features an active tip angled at 25 degrees, optimized for delicate oral surgery interventions. This device is delivered non-sterile by the manufacturer and requires a complete preparation protocol before any clinical use. It is a robust tool intended for repeated use after appropriate reprocessing.

What are the clinical indications?

This angled sinus elevator is primarily indicated for pre-implant surgery procedures, notably sinus membrane elevation (sinus lift). Its role is crucial when creating space for the insertion of bone substitutes under the Schneiderian membrane. The 25 degrees angulation allows the practitioner to navigate with precision along the internal walls of the maxillary sinus, facilitating membrane detachment without perforation. It is exclusively reserved for use by health professionals qualified in oral surgery and implantology, thus guaranteeing handling in accordance with clinical requirements.

What are the technical characteristics?

The Helmut Zepf 41.868.01 instrument is distinguished by its manufacture in high-quality medical stainless steel, ensuring resistance to corrosion and increased longevity. Its major technical feature lies in its 25 degrees tilt, offering an optimal angle of attack for posterior sectors. As a Class I device, it meets safety requirements for non-invasive or short-term invasive manual instruments. The design is studied to withstand repeated cycles of cleaning, disinfection, and sterilization without alteration of its mechanical properties, although no maximum cycle limit is defined by the manufacturer.

What are the contraindications for use?

The main contraindication related to the use of this instrument is the patient's known hypersensitivity or intolerance to metals, specifically medical stainless steel. A hypersensitivity reaction may be triggered upon contact with tissues. If such a reaction occurs during the intervention, the manufacturer Helmut Zepf specifies that the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any manipulation. Additionally, use is contraindicated if the instrument shows visible damage such as cracks or defects on the edges.

What are the maintenance and sterilization precautions?

As the instrument is delivered non-sterile, complete cleaning, disinfection, and sterilization are mandatory before the first use and after each subsequent use. The practitioner must carefully inspect the elevator to detect any trace of wear, corrosion, or breakage before intervention. The use of damaged products is strictly prohibited. Due to the quality of materials used by Helmut Zepf Medizintechnik GmbH, there is no predefined limit on the number of reprocessing cycles, but compatibility with other cleaning products and autoclave parameters must be verified beforehand by the user.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects manufacturing standards for manual dental instruments. The product is classified as a Class I medical device according to current regulations. The safety and use instructions provided by the manufacturer emphasize the importance of compliance with sterilization protocols and traceability. Each instrument is identified by a unique technical reference (41.868.01) allowing precise tracking within the dental office or hospital structure, thus guaranteeing the safety of the patient and the practitioner.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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