Elevator X - LUXA - TOOL - 6 - Helmut Zepf (17.007.06) - Delynov
Optimize your dental extractions with the Helmut Zepf X-TOOL elevator
Designed to lift teeth and residual roots with precision, this manual instrument ensures efficient handling during surgical procedures.
- Model: X-TOOL 6 (Reference 17.007.06).
- Configuration: 3.0 mm straight tip.
- Material: Biocompatible medical stainless steel.
- Safety: Class Ir device, delivered non-sterile and autoclavable.
Product features
The Elévateur X - LUXA - TOOL - 6 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.007.06.
- 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
Instrument dentaire manuel utilisé pour soulever les dents ou les racines dentairesrésiduelles lors de l'extraction d'une dent. 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 Elévateur X - LUXA - TOOL - 6 - Helmut Zepf?
The Elévateur X - LUXA - TOOL - 6, referenced under code 17.007.06 by Helmut Zepf, is a high-precision manual dental instrument designed for extraction surgery. This device is manufactured from medical stainless steel, ensuring the robustness necessary for oral surgery interventions. As an instrument from the brand Helmut Zepf Medizintechnik GmbH, it is distinguished by its ergonomic design facilitating grip and the application of force during clinical procedures. This device belongs to Class I of medical devices, which confirms its compliance with basic regulatory requirements for non-invasive or minimally invasive instruments used in dental practices by qualified practitioners.
What are the clinical indications for this instrument?
The intended use of this Helmut Zepf instrument is specifically defined for tooth extraction procedures. It is indicated for lifting teeth or extracting residual dental roots effectively. Its role is crucial for facilitating initial luxation before the use of forceps or for finalizing the extraction of complex root fragments. This device is exclusively reserved for professional use by healthcare practitioners trained in dental and oral surgery techniques. The use of this tool allows for minimizing alveolar trauma during elevation maneuvers, provided that standard operating protocols in force in the field of odontology are respected.
What are the technical characteristics of the 17.007.06 elevator?
The X-TOOL 6 elevator (reference 17.007.06) features technical characteristics optimized for daily surgical practice. Manufactured in medical stainless steel, it offers high resistance to deformation and corrosion. This material allows for repeated reprocessing without loss of immediate mechanical properties, although it is imperative to check for the absence of visible damage such as cracks, breaks, or defects on the cutting edges before each intervention. The manufacturer Helmut Zepf specifies that due to the design and materials used, there is no defined maximum limit of treatment cycles, as long as the integrity of the instrument is preserved and confirmed by rigorous visual inspection.
What are the contraindications for the use of this device?
The main contraindication related to the use of this medical stainless steel instrument concerns metal intolerance in the patient. Contact with the instrument may trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken accordingly. Furthermore, it is strictly forbidden to use products showing visible damage or wear, such as blunt edges or micro-cracks, as this could compromise patient safety or extraction efficiency. Use is strictly limited to qualified healthcare professionals.
What are the maintenance and sterilization precautions?
Helmut Zepf instruments are delivered non-sterile and must imperatively follow a complete preparation protocol before the first use and after each subsequent use. The reprocessing cycle necessarily includes thorough cleaning, disinfection, and sterilization. It is crucial to clean each product before its use to guarantee the elimination of any residue. Before each cycle, the practitioner must check compatibility with other products and inspect the instrument to detect any wear. The use of damaged instruments is prohibited. Compliance with these manufacturer safety instructions is essential to maintain the performance of the medical stainless steel and ensure asepsis during surgical interventions.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures the traceability and quality of its products through rigorous manufacturing processes. As a Class I device, it meets the safety and performance standards applicable to manual dental instruments. Professionals can refer to the manufacturer's instructions for reprocessing and use, thereby ensuring practice in accordance with public health and patient safety requirements within the framework of dental and surgical care.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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