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Instrument Sinus-Lift Fig. 2 - Helmut Zepf (41.847.01)

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The Instrument Sinus-Lift Fig. 2 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.847.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

93.81 € 93.81 EUR 93.81 € Tax Included

93.81 € Tax Included

(93.81 € / Units)
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Instrument

What is the Sinus-Lift Fig. 2 - Helmut Zepf instrument?

The Sinus-Lift Fig. 2 instrument, referenced under code 41.847.01, is a manual dental instrument developed by the manufacturer Helmut Zepf Medizintechnik GmbH. Specifically designed for oral surgery, this tool is manufactured from high-quality medical stainless steel to ensure optimal resistance during surgical manipulations. Its structure is designed to meet the requirements of pre-implant surgery interventions, offering ergonomics adapted to the needs of practitioners. As a Class I device, it meets the regulatory standards for non-invasive or invasive instruments for temporary use, ensuring constant reliability during sinus membrane elevation.

What are the clinical indications for this instrument?

This instrument is primarily indicated for sinus lift procedures in implantology and oral surgery. Its main role is to assist in the detachment and elevation of the Schneiderian membrane to create the space necessary for the insertion of bone filling materials. Sinus instrumentation with Fig. 2 allows for precise work along the bony walls of the maxillary sinus. It is exclusively reserved for use by qualified healthcare professionals trained in implant and periodontal surgery techniques, thereby ensuring a safe application in compliance with current clinical protocols.

What are the technical characteristics of the 41.847.01 instrument?

The Sinus-Lift Fig. 2 instrument from Helmut Zepf is distinguished by its medical stainless steel construction, a material chosen for its mechanical properties and biocompatibility. This manual device is designed to be reusable after a complete reprocessing cycle. The specific design of Fig. 2 allows for precise manipulation during the critical stages of sinus elevation. It is important to note that the product is delivered non-sterile by Helmut Zepf Medizintechnik GmbH. Before each use, the practitioner must perform a visual inspection to detect any damage, cracks, or wear on the edges, as the use of damaged products is strictly prohibited.

What are the contraindications for the use of this device?

The main medical contraindication mentioned by the manufacturer concerns hypersensitivity or metal intolerance. Being made of medical stainless steel, any contact with the patient can trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. Apart from this material-related contraindication, the use of the instrument is limited by the physical condition of the tool: any sign of visible wear, breakage, or defect on the active parts constitutes a contraindication to its use to ensure patient safety.

What are the maintenance and sterilization precautions?

Like any Helmut Zepf surgical instrument, this device must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. The cleaning process must be complete to eliminate any biological residue. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit for treatment cycles, as long as the instrument does not show visible damage. It is crucial to check for the absence of corrosion or deformation before each cycle. Strict compliance with standard sterilization protocols for medical stainless steel is essential to maintain asepsis and the longevity of the sinus instrumentation.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its products with safety and performance requirements. The instructions provided emphasize the importance of respecting reprocessing procedures and monitoring the condition of the instrument to ensure use in accordance with the intended purpose. As a manual precision instrument, it benefits from Helmut Zepf's expertise in the field of dental instrumentation, providing professionals with a reliable tool for their daily surgical interventions.


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Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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