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DISSECTION FORCEPS - Helmut Zepf (22.230.14) - Delynov

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The PINCES A DISECTION. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 22.230.14.
  • Reserved for healthcare professionals. Read instructions carefully before use.

41.14 € 41.14 EUR 41.14 € Tax Included

41.14 € Tax Included

(41.14 € / Units)
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Instrument

What are the Helmut Zepf (22.230.14) dissection forceps?

Helmut Zepf dissection forceps, referenced under code 22.230.14, are precision instruments designed for the delicate manipulation of tissues during surgical procedures. This medical device, distributed by Delynov, belongs to the category of guided bone regeneration (GBR) instruments. Manufactured by Helmut Zepf Medizintechnik GmbH, these forceps benefit from the expertise of a manufacturer renowned for the quality of its dental instrumentation. They allow for secure gripping and optimal control during dissection phases, thus facilitating the practitioner's work in restricted anatomical areas requiring great finesse of execution.

What are the clinical indications for this instrument?

These dissection forceps are primarily indicated for oral surgery, implantology, and guided bone regeneration (GBR) procedures. They are used for spreading, grasping, and manipulating soft tissues without excessive trauma. Their design allows dental surgeons and implantologists to perform precise flap dissections, thereby promoting clear exposure of the surgical site. The use of this Helmut Zepf instrument is essential for maintaining tissue integrity during critical steps of implant site preparation or the placement of filling materials.

What are the technical characteristics of reference 22.230.14?

Technical reference 22.230.14 corresponds to a specific model of dissection forceps within the Helmut Zepf catalog. Although exact dimensions are not specified in the source data, this instrument is designed to meet the ergonomic requirements of oral health professionals. Its structure is optimized to offer a perfect balance between lightness and robustness, guaranteeing precise transmission of the force exerted by the surgeon. The instrument's finish is designed to limit reflections under surgical lighting, thus ensuring increased visual comfort during prolonged dental surgery interventions.

What are the contraindications for the use of these forceps?

The use of Helmut Zepf dissection forceps does not present specific contraindications beyond those related to standard surgical protocols in the oral environment. However, it is imperative not to use this instrument for tasks for which it is not intended, such as manipulating rigid materials or metal wires that could damage the precision jaws. The practitioner must ensure the absence of serious systemic pathologies in the patient that could contraindicate surgical intervention. One should systematically refer to the instructions for use provided by the manufacturer to know the specific usage limits.

What are the maintenance precautions for this non-resorbable instrument?

As a reusable surgical instrument, the Helmut Zepf dissection forceps require a strict cleaning and sterilization protocol after each use. Although specific processing details are not listed here, it is recommended to follow standard hospital decontamination guidelines and the instructions from the manufacturer Helmut Zepf Medizintechnik GmbH. Regular inspection of the instrument is necessary to check for the absence of corrosion or deformation of the dissection jaws. Rigorous maintenance guarantees the longevity of the tool and patient safety during implant surgery and bone regeneration procedures.

Who is the manufacturer and what is the regulatory information?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a German company specializing in high-quality medical instrumentation. The product is identified under reference 22.230.14 and is distributed by Delynov. Regarding regulatory aspects such as the device class or CE marking, the source data does not specify this information. It is therefore advised that healthcare professionals consult the product labeling and the technical documentation accompanying the device to verify its compliance with current standards and its specific conditions of use according to 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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