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Elevator sinus 120 degrees - Helmut Zepf (41.868.04) - Delynov

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The Élévateur sinus 120 degrés - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.868.04.
  • Reserved for healthcare professionals. Read instructions carefully before use.

120.80 € 120.8 EUR 120.80 € Tax Included 236.57 €

120.80 € Tax Included 236.57 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf 120-degree sinus elevator?

The 120-degree sinus elevator, referenced under code 41.868.04 by Helmut Zepf, is a specialized manual surgical instrument. Manufactured from high-quality medical stainless steel, this instrument is designed for complex oral surgery interventions. Its structure is characterized by a working end oriented at 120 degrees, allowing the practitioner to reach specific anatomical areas during sinus augmentation procedures. As a Class I device, it meets the safety requirements for reusable instruments, requiring a complete cycle of cleaning, disinfection, and sterilization before each use to guarantee the asepsis of the operating field.

What are the clinical indications?

This 120-degree sinus elevator is primarily indicated during pre-implant surgeries, specifically for sinus lifting (sinus lift). It is used by dental surgeons and implantologists to delicately detach the Schneiderian membrane from the internal bony wall of the maxillary sinus. Its use extends to any surgical work on the dental apparatus requiring precise manual instrumentation in stainless steel. The instrument allows for the creation of the space necessary for the insertion of bone grafting materials, thus facilitating subsequent implant rehabilitation in atrophied posterior sectors.

What are the technical characteristics?

The Helmut Zepf elevator (41.868.04) is entirely designed in medical stainless steel, a material chosen for its resistance to thermal and chemical treatment cycles. Its main characteristic lies in its 120-degree angulation, optimized for ergonomics when accessing sinus walls. The manufacturer, Helmut Zepf Medizintechnik GmbH, delivers this product non-sterile. It is the responsibility of the healthcare professional to check the condition of the instrument before each use, ensuring the absence of visible damage such as cracks, breaks, or defects on the active parts, in order to maintain the integrity of the manipulated tissues.

What are the contraindications for use?

The main contraindication related to the use of this instrument is known hypersensitivity or intolerance of the patient to metals, particularly to the components of medical stainless steel. In the event of a hypersensitivity reaction triggered during contact with the instrument, the surgical procedure must be immediately interrupted and the necessary medical measures must be taken. Furthermore, the use of the instrument is strictly prohibited if it shows visible signs of wear, cracks, or defects on the edges, as this could compromise patient safety and the effectiveness of the surgical procedure.

What are the maintenance and reprocessing precautions?

As a reusable medical device, all Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer emphasizes that it is crucial to clean each product before proceeding with sterilization. Due to the robust design and materials used (stainless steel), there is no defined maximum limit of treatment cycles, as long as the instrument does not show functional degradation. The practitioner must verify compatibility with other products used and ensure that the instrument is perfectly dry and free of residues before storage.

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 rigorous manufacturing standards for surgical instruments. The product is classified as a Class I medical device according to current regulations. Each instrument is identified by a unique technical reference (41.868.04) ensuring its traceability. The manufacturer's safety instructions specify that the use of this instrument is exclusively reserved for qualified healthcare professionals, guaranteeing an application in accordance with the state of the art in dental and implant surgery.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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