Surgical dental extraction forceps figure 18 for upper molars - Helmut Zepf (15.218.00D) - Delynov
The Davier chirurgical figure 18 pour extractions de molaires supérieures - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 15.218.00D.
- Reserved for healthcare professionals. Read instructions carefully before use.
What are the Helmut Zepf figure 18 surgical forceps?
The Helmut Zepf surgical forceps, bearing reference 15.218.00D, are a manual instrument used for exodontia. This model, identified as figure 18, features a structure designed to adapt to the specific morphology of molars located in the upper arch. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is intended for the practice of oral surgery and implantology. Its design allows for efficient transmission of the force necessary to rupture the alveolar-dental ligament fibers. This tool is part of the range of high-precision instruments for simple or complex extraction procedures.
What are the clinical indications for these extraction forceps?
The use of these surgical extraction forceps is indicated for the avulsion of upper molars. In clinical practice, they are used by the dental surgeon or oral surgeon when the extraction of a maxillary molar is necessary, whether for reasons of non-restorable caries, terminal periodontitis, root fracture, or as part of a pre-implant treatment plan. Their shape is designed to grip the dental crown at the neck, thus allowing the rotational and lateral movements essential for widening the socket and the final extraction of the tooth.
What are the technical characteristics of model 15.218.00D?
The Helmut Zepf reference 15.218.00D forceps are distinguished by their beak geometry specifically adapted to upper molars. Figure 18 corresponds to a curvature and orientation of the beaks that facilitate access to the posterior areas of the maxilla. The instrument is designed to provide a stable grip, limiting the risk of slipping during the application of traction forces. Like the entire Helmut Zepf range, this device is developed to meet the sterilization and durability requirements necessary in a surgical environment, thus ensuring constant performance during repeated interventions in the dental office.
What are the contraindications for the use of this instrument?
Contraindications for the use of these surgical forceps are mainly related to the patient's clinical condition and the structure of the tooth to be extracted. They must not be used on teeth located in the mandible or on anterior teeth, for which other forceps figures are required. Furthermore, their use may be contraindicated in cases of significant risk of bone fracture if the socket is too dense, then requiring an alveolectomy approach. It is the practitioner's responsibility to evaluate the risks of post-operative complications and to ensure the absence of general medical contraindications in the patient before any exodontia procedure.
What are the maintenance precautions for this non-resorbable equipment?
As a reusable metallic surgical instrument, the Helmut Zepf forceps require a strict protocol of decontamination, cleaning, and sterilization after each use. It is imperative to follow the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH regarding autoclave cycles and compatible cleaning products in order to prevent corrosion and maintain the functional integrity of the beaks and the joint. A visual inspection before each procedure is recommended to check for the absence of residues or structural damage that could compromise patient safety or the effectiveness of the surgical act.
Who is the manufacturer and what standards are respected?
This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of dental and surgical instrumentation. Although detailed regulatory specifications such as the exact class or CE marking are not explicitly mentioned in this technical sheet, Helmut Zepf products are designed according to rigorous industrial quality standards. For any precise information regarding certifications, applied ISO standards, or details of compliance with the European Medical Device Regulation (MDR), it is recommended to refer to the official technical documentation provided by the manufacturer or to consult the instructions for use attached to the product.
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| Manufacturer | Helmut Zepf |
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