DENTAL EXTRACTION FORCEPS. ENGLISH PATTERN FIGURE 22 - Helmut Zepf (12.022.00Z) - Delynov
The DAVIER. FORME ANGLAISE FIGURE 22 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 12.022.00Z.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf figure 22 extraction forceps?
The Helmut Zepf extraction forceps (reference 12.022.00Z) is a manual dental instrument of English pattern figure 22. It is manufactured from high-quality medical stainless steel, a standard material for surgical instrumentation ensuring resistance to decontamination processes. This device is specifically designed for oral surgery interventions requiring a robust grip. As a Class I instrument, it meets the regulatory requirements for non-invasive or invasive medical devices for temporary use. Its structure is designed to meet the needs of practitioners during extractions in the lower arch.
What are the clinical indications?
This forceps is indicated for lower molar extraction within the framework of dental and implant surgery. It is used by healthcare professionals for the avulsion of mandibular teeth when the condition of the tooth or root requires the use of specific extraction forceps. Its clinical application is limited to odontostomatology procedures performed in a private practice or hospital setting. The instrument allows the molar to be grasped at the neck to apply the luxation and avulsion movements necessary for its removal from the socket, while respecting the surrounding tissues according to current surgical protocols.
What are the technical characteristics?
The Helmut Zepf 12.022.00Z forceps is characterized by its English pattern figure 22, adapted to the anatomy of lower molars. Manufactured by Helmut Zepf Medizintechnik GmbH, it is composed of medical stainless steel. This material is chosen for its ability to undergo repeated cleaning and sterilization cycles. The instrument is delivered non-sterile and must undergo complete processing before its first use and after each subsequent use. The product design and materials used do not allow for a defined maximum limit of processing cycles, although visible wear must be systematically checked by the practitioner.
What are the contraindications for use?
The main medical contraindication mentioned by the manufacturer concerns hypersensitivity or intolerance to metals. Contact with the medical stainless steel instrument can cause an allergic reaction in certain sensitive patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the surgical procedure.
What are the maintenance and safety precautions?
All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each surgical procedure. It is crucial to clean each product before use to remove any residue. The practitioner must inspect the instrument to detect any signs of wear or visible damage (cracks, jaw defects). A damaged product must never be used. Since the device is delivered non-sterile, strict compliance with the reprocessing protocol is mandatory. The use of this forceps is strictly reserved for qualified healthcare professionals trained in lower molar extraction techniques and the handling of associated rotary or manual instrumentation.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This forceps is classified as a Class I medical device according to the regulations in force. The manufacturer guarantees the traceability and quality of the medical stainless steel used for the manufacture of its instruments. Compliance with the cleaning and sterilization instructions recommended by Helmut Zepf is essential to maintain product conformity throughout its life cycle. As a Class I device, it meets the safety and performance standards required for manual instrumentation in dental surgery.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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