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Kocher-Langenbeck - Bone Forceps Helmut Zepf (38.426.06)

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The Kocher-Langenbeck - Pince à os Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 38.426.06.
  • Reserved for healthcare professionals. Read instructions carefully before use.

70.60 € 70.6 EUR 70.60 € Tax Included

70.60 € Tax Included

(70.60 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf Kocher-Langenbeck bone forceps?

The Helmut Zepf Kocher-Langenbeck bone forceps is a specialized surgical instrument used primarily in oral and maxillofacial surgery. This device, identified under reference 38.426.06, belongs to the category of guided bone regeneration (GBR) instruments. Its structure is designed to offer a robust grip on hard tissues, allowing the practitioner to manipulate bone segments with great stability. Manufactured by Helmut Zepf Medizintechnik GmbH, this kocher bone forceps is distinguished by its ergonomic design adapted to the requirements of clinical environments specialized in implantology.

What are the clinical indications for this instrument?

The kocher langenbeck forceps is indicated for various oral surgery procedures requiring the manipulation of bone structures. In implantology, it is used during bone grafts to hold blocks or cortical fragments in position before fixation. It is also relevant in alveolar ridge regularization procedures or during the excision of bone segments. Its primary function is to ensure a secure grip, preventing the instrument from slipping on the hard, smooth surfaces of the bone, which is crucial for the precision of the surgical gesture during reconstruction phases.

What are the technical characteristics of the 38.426.06 forceps?

The Kocher-Langenbeck bone forceps, bearing technical reference 38.426.06, features specific characteristics of the Helmut Zepf range dedicated to GBR. Although exact dimensions are not specified, its morphology meets the standards of classic Kocher-Langenbeck forceps, characterized by robust jaws and a ratchet locking system. This mechanism allows for maintaining constant pressure without continuous manual effort, thus facilitating the work of the assistant or surgeon during the exposure of the surgical site or the stabilization of a bone graft.

What are the contraindications for the use of this instrument?

There are no documented specific medical contraindications for the use of the Kocher-Langenbeck bone forceps, other than those related to standard surgical protocols. However, its use must be limited to the tissues for which it was designed, namely hard tissues or bone fragments. Inappropriate use on fragile structures, nerves, or blood vessels could lead to tissue damage. As with any surgical instrument, the practitioner must ensure the absence of known patient allergies to the metallic components of the instrumentation before any intervention.

What are the maintenance precautions for this bone forceps?

As a reusable surgical instrument from the Helmut Zepf brand, the kocher bone forceps must undergo a rigorous sterilization protocol after each use. Although resorption details do not apply here, the longevity of the instrument depends on compliance with cleaning, disinfection, and autoclave sterilization cycles. It is recommended to use non-corrosive cleaning solutions and to regularly check the integrity of the ratchet and jaws to ensure optimal functionality during guided bone regeneration surgeries.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-precision dental and surgical instrumentation. The Kocher-Langenbeck bone forceps (38.426.06) is produced according to the German company's quality standards. For any specific information regarding the regulatory class, CE marking, or ISO certifications applicable to this specific model, it is imperative to refer to the instructions for use provided by the manufacturer or the product labeling, in accordance with the requirements of the European Medical Device Regulation.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Helmut Zepf
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