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Dental extraction forceps for upper molars, figure 18, Exlog - Helmut Zepf (15.218.00) - Delynov

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The Davier pour extraction de molaires supérieures, figure 18, Exlog - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 15.218.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

177.46 € 177.46 EUR 177.46 € Tax Included

177.46 € Tax Included

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Instrument

What is the Helmut Zepf upper molar extraction forceps?

The upper molar extraction forceps, referenced under code 15.218.00, is a manual instrument from the Exlog range developed by Helmut Zepf Medizintechnik GmbH. This device belongs to the category of instrumentation consumables for oral surgery. Its structure is designed to offer a stable and secure grip during extraction maneuvers in the maxilla. As an instrument of the Exlog series, it benefits from Helmut Zepf's expertise in designing tools dedicated to exodontia, aiming to meet the daily requirements of dental practices and implant surgery centers.

What are the clinical indications for this instrument?

The primary use of this forceps concerns the avulsion of upper molars. In dental and oral surgery, this instrument is indicated when the practitioner must proceed with the extraction of a multi-rooted tooth from the upper arch, whether for reasons of non-restorable caries, terminal periodontitis, or as part of a pre-implant treatment plan. Figure 18 is a standardized shape recognized for its effectiveness on the posterior maxillary sectors. It allows for the application of the rotational and traction forces necessary to rupture the alveolar-dental ligament while respecting the integrity of the surrounding bone tables.

What are the technical characteristics of the 15.218.00 forceps?

The Helmut Zepf extraction forceps, figure 18, features morphological characteristics specific to the anatomy of the upper molars. The design of its beaks is intended to adjust perfectly to the bifurcation of the maxillary roots, thus ensuring optimal force transmission without slipping. Technical reference 15.218.00 corresponds to a model from the Exlog line, characterized by a surface finish and handle ergonomics that promote grip, even in a wet environment. This instrument is designed to withstand repeated cleaning and sterilization cycles in an autoclave, in accordance with the hygiene protocols in force in healthcare facilities.

What are the contraindications for the use of this device?

The contraindications for the use of this upper molar extraction forceps are mainly related to the patient's clinical state and root morphology. It must not be used on mandibular teeth or anterior teeth for which its shape is not adapted, at the risk of causing root fractures or soft tissue lesions. Furthermore, the use of this instrument is contraindicated in patients presenting general contraindications to surgical extraction (uncontrolled hemostasis disorders, recent local irradiation, etc.). Reference should systematically be made to the manufacturer's recommendations from Helmut Zepf to ensure safe use.

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

As a reusable steel surgical instrument, the Helmut Zepf forceps requires a rigorous maintenance protocol to prevent corrosion and cross-contamination. After each procedure, the instrument must be decontaminated, cleaned (manually or by ultrasound), and dried before being packaged for sterilization. It is crucial to use neutral pH cleaning solutions to preserve the integrity of the metal. The practitioner must regularly inspect the beaks and the hinge of the 15.218.00 forceps to detect any sign of wear or deformation that could compromise the safety of the operative procedure during the extraction of upper molars.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the field of high-precision dental instrumentation. Although specific details of the CE marking and regulatory class are not explicitly mentioned in the source data for this reference 15.218.00, Helmut Zepf products are generally manufactured according to high quality standards specific to the German medical industry. For any precise information regarding compliance with the European Medical Device Regulation (MDR), it is imperative to consult the instructions for use provided by the manufacturer or to contact the Delynov technical service.


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Manufacturer Helmut Zepf
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