Extracting Forceps, English Pattern, Fig. 79 - Helmut Zepf (12.279.90ZTI) - Delynov
The DAVIER. FORME ANGL.. FIG. 79 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 12.279.90ZTI.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf FIG. 79 forcep?
The Helmut Zepf FIG. 79 forcep (reference 12.279.90ZTI) is a manual plier-type surgical instrument designed for dental extraction. Manufactured from high-quality medical stainless steel, this device features a specific English pattern adapted to mandibular anatomy. It belongs to the category of reusable consumables (CONSO) and is distinguished by its structural robustness. This instrument is delivered non-sterile and requires a complete preparation protocol before any intervention. It is exclusively reserved for use by qualified healthcare professionals in dental and oral surgery.
What are the clinical indications for this root forcep?
This root forcep is indicated for exodontia procedures, specifically for the extraction of teeth and roots located on the lower arch. In clinical practice, the forcep 79 is used to firmly grasp the dental or root structure in order to apply the necessary luxation and avulsion forces. Its ergonomic English pattern design allows effective access to the posterior areas of the mandible. It is used during simple or complex extraction surgeries where precise gripping of the lower root is required to finalize alveoloplasty or prepare a future implant site.
What are the technical characteristics of this instrument?
The Helmut Zepf FIG. 79 forcep is characterized by its medical stainless steel composition, guaranteeing mechanical resistance adapted to extraction constraints. Identified under code 12.279.90ZTI, it features a robust articulated architecture allowing for optimal transmission of manual force. As a Class I device, it meets the regulatory safety requirements for non-invasive or temporary-use invasive surgical instruments. Its design allows for repeated reprocessing, including cleaning, disinfection, and sterilization, without a defined maximum limit of cycles, subject to the absence of visible damage during inspection.
What are the contraindications for the use of this device?
The main medical contraindication for using this forcep is the patient's known hypersensitivity or intolerance to metals, particularly to the components of medical stainless steel. In the event of an allergic reaction or hypersensitivity triggered upon contact with the instrument, the manufacturer Helmut Zepf Medizintechnik GmbH recommends immediate cessation of the procedure and the implementation of appropriate medical measures. Furthermore, use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, to ensure the safety of both the patient and the practitioner.
What are the maintenance and sterilization precautions?
All instruments supplied by Helmut Zepf must imperatively be cleaned, disinfected, and sterilized before the first use as well as after each subsequent use. The reprocessing process must be complete to ensure asepsis. Before each intervention, the practitioner must perform a rigorous visual inspection to detect any signs of wear, corrosion, or deformation. It is crucial never to use a damaged product. Although the material allows for many processing cycles, the longevity of the forcep depends on strict compliance with cleaning protocols and systematic verification of the integrity of the beaks and the joint.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This forcep is classified as a Class I medical device according to current regulations. The manufacturer ensures the instrument's compliance with quality standards for medical stainless steel. Helmut Zepf products are delivered non-sterile, placing responsibility on the healthcare professional for the validation of the sterilization cycle before use. Compliance with the instructions for use and safety provided by the manufacturer is essential to maintain the compliance and clinical safety of the device during extractions.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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