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Elevator X - Luxa - Tool - Curved - 4 - Helmut Zepf (17.007.04)

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The Élévateur X - Luxa - Instrument - Courbé - 4 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 17.007.04.
  • Reserved for healthcare professionals. Read instructions carefully before use.

79.04 € 79.04 EUR 79.04 € Tax Included 170.43 €

79.04 € Tax Included 170.43 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf X-Luxa Elevator?

The X-Luxa Elevator, referenced under code 17.007.04, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this INSTRU category tool features a curved structure adapted to the requirements of oral surgery. It is part of the Class I devices, meeting the manufacturer's rigorous standards for dental extraction. Its stainless steel composition ensures compatibility with the cleaning and sterilization processes required in a clinical environment, while providing the necessary resistance to the leverage forces applied during interventions.

What are the clinical indications for this instrument?

The intended use of this Helmut Zepf instrument is specifically defined for exodontia procedures. It is indicated as a manual instrument used to lift teeth or residual dental roots during tooth extraction. In oral surgery, its role is essential for breaking ligament attachments and mobilizing the tooth or remaining root fragments in the socket. Its use is strictly reserved for qualified healthcare professionals, ensuring handling in accordance with current clinical protocols to minimize post-operative complications.

What are the technical characteristics of elevator 17.007.04?

The X-Luxa elevator (17.007.04) is distinguished by its curved configuration (model 4), optimized for precise working ergonomics in the mouth. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. As a Class I device, it is designed to be reusable. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit of processing cycles, although a visual inspection before each use is mandatory to detect any wear or damage.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer concerns hypersensitivity to the instrument's components. Metal intolerance in the patient may result from direct contact with the medical stainless steel constituting the elevator. If a hypersensitivity reaction is triggered during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any manipulation. Furthermore, the use of an instrument showing visible damage, such as cracks, breaks, or defects on the cutting edges, is strictly prohibited.

What are the maintenance and safety precautions?

Patient safety and the longevity of the Helmut Zepf instrument depend on a strict maintenance protocol. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to check the condition of the elevator before each intervention: the presence of cracks or marked wear on the working part makes the device unfit for use. In case of visible damage, the instrument must never be used. Reprocessing must follow the manufacturer's guidelines to ensure that the stainless steel retains its mechanical properties and corrosion resistance throughout the sterilization cycles.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with the regulatory requirements relating to Class I medical devices. The products are delivered non-sterile, engaging the responsibility of the healthcare professional regarding their preparation before use. Traceability is ensured by the technical reference 17.007.04. Compliance with the cleaning and sterilization instructions issued by Helmut Zepf is essential to maintain the device's conformity and ensure the safety of care during complex or simple dental extractions.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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