Beyer Bone Rongeur - Helmut Zepf (42.650.18) - Delynov
Product features
The Pince-Gouge Beyer - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 42.650.18.
- Reserved for healthcare professionals. Read instructions carefully before use.
fabricant : HELMUT ZEPF Medizintechnik Gmbh , Obere Hauptstraße 16-22, D- 78606 Seitingen-Oberflacht BUT PRÉVU / INDICATION Un instrument chirurgical doté de tiges stables pour couper ou écraser les os pendant une intervention chirurgicale. Les effets secondaires indésirables l'intolérance aux métaux chez le patient peut résulter d'un contact avec l'instrument, qui est en acier inoxydable médical une réaction d'hypersensibilité était toujours déclenchée devenir. la procédure doit être arrêtée si une telle réaction se produit et les mesures nécessaires sont prises en conséquence. consignes d'utilisation et de sécurité tous les instruments doivent être nettoyés avant d'être utilisés pour la première fois et compléter avant toute utilisation ultérieure nettoyé, désinfecté et stérilisé ! il est très important de nettoyer chaque produit avant utilisation dommages et usures visibles, par ex. b. fissures, cassures ou des défauts sur les arêtes de coupe. n'utilisez jamais de produits endommagés ou usés. les produits de helmut zepf medizintechnik gmbh sont livrés non stériles. les produits doivent être à l'avance nettoyé et stérilisé. la compatibilité aussi les autres produits doivent être vérifiés au préalable. retraitement en raison de la conception du produit, des matériaux utilisés et il ne peut y avoir de limite maximale définie pour l'utilisation prévue des cycles de traitement réalisables peuvent être déterminés.réservé aux professionnels de santé.
What is the Beyer bone rongeur by Helmut Zepf?
The Beyer bone rongeur, referenced under code 42.650.18 by Helmut Zepf, is a high-precision surgical instrument designed for bone manipulation. Manufactured from high-quality medical stainless steel, it consists of stable shanks allowing for optimal force transmission during the operative act. This device belongs to the category of Guided Bone Regeneration (GBR) instruments. Its robust structure guarantees reliable handling for demanding practitioners. As a Class I medical device, it meets the safety and performance requirements for oral surgery interventions. This instrument is delivered non-sterile and requires a complete preparation protocol before its first use in the practice or operating theater.
What are the clinical indications for this instrument?
The intended use of the Beyer bone rongeur from Helmut Zepf Medizintechnik GmbH is specifically defined for surgical interventions requiring the cutting or crushing of bone tissue. It is indicated in bone surgery protocols where precise ridge reduction or bone modeling is necessary. The stable shanks of the instrument allow the surgeon to work with great control during bone resection. This instrument is an essential tool in implantology and oral surgery for preparing the recipient site or adjusting bone volumes. Its use is strictly reserved for qualified healthcare professionals, thus guaranteeing application in accordance with the rules of surgical art.
What are the technical characteristics of the 42.650.18 bone rongeur?
The Beyer bone rongeur (42.650.18) is distinguished by its ergonomic design and its manufacture in medical stainless steel, a material chosen for its resistance and durability. The main technical characteristics lie in its stable shanks which ensure effective cutting or crushing action without deformation of the instrument. Helmut Zepf designed this tool to withstand repeated processing cycles without a defined maximum limit, subject to compliance with maintenance protocols. Before each use, the practitioner must imperatively inspect the instrument to detect any visible damage, such as cracks, breaks, or defects on the cutting edges. The absence of such defects is crucial to guarantee cutting performance and patient safety.
What are the contraindications for the use of this instrument?
The main contraindication for the use of the Beyer bone rongeur lies in metal intolerance. Contact with this medical stainless steel instrument can trigger a hypersensitivity reaction in certain sensitive patients. If such an intolerance reaction occurs during the intervention, the manufacturer Helmut Zepf Medizintechnik GmbH stipulates that the procedure must be immediately stopped in order to take the necessary medical measures. Furthermore, the use of the instrument is formally contraindicated if it shows visible signs of wear, cracks, or damage to the active parts. Use is also exclusively reserved for trained healthcare professionals, excluding any use by unqualified persons.
What are the maintenance and sterilization precautions?
As a non-resorbable and reusable device, the Beyer bone rongeur requires a rigorous maintenance protocol. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. Thorough cleaning is a critical step before sterilization to ensure the elimination of all biological residues. The manufacturer emphasizes the importance of verifying compatibility with other products used simultaneously. Due to the robust design and materials used, there is no defined maximum limit of processing cycles, but the lifespan depends directly on the absence of visible damage. Any instrument showing defects on the cutting edges or signs of structural fatigue must be removed from the clinical circuit.
Who is the manufacturer and what standards are respected?
The Beyer bone rongeur is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This manufacturer is recognized for its expertise in the production of high-precision surgical instruments. The device is classified as Class I according to the current regulations on medical devices. It is designed to meet the strict safety and performance requirements expected by dental surgeons and implantologists. Each product is delivered with detailed safety instructions concerning its cleaning, disinfection, and sterilization. Compliance with these manufacturer guidelines ensures the longevity of the instrument and the safety of the care provided to patients within healthcare facilities.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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