Elevator X-LUXATOOL 1 - Helmut Zepf (17.007.01TI) - Delynov
The Élévateur X-LUXATOOL 1 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.007.01TI.
- 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 Helmut Zepf X-LUXATOOL 1 elevator?
The X-LUXATOOL 1 elevator, reference 17.007.01TI, is a high-precision manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. This medical device is manufactured from medical-grade stainless steel, ensuring robustness suited to the requirements of oral surgery. As a Class I instrument, it is specifically developed to assist practitioners during the delicate phases of tooth extraction. Its structure is optimized to offer reliable and secure handling, meeting the rigorous standards of healthcare professionals seeking durable tools for their daily practice in dental offices or hospital environments.
What are the clinical indications for this instrument?
The intended use of this Helmut Zepf instrument is clearly defined for tooth extraction procedures. It is indicated as a manual instrument for lifting teeth or residual dental roots. Its role is crucial for facilitating the luxation and elevation of dental structures before their final removal from the socket. This device is intended exclusively for qualified healthcare professionals, such as dental surgeons and implantologists, who perform simple or complex extractions requiring precise instrumentation to minimize trauma to surrounding tissues during root mobilization.
What are the technical characteristics of the 17.007.01TI elevator?
The X-LUXATOOL 1 elevator (reference 17.007.01TI) is distinguished by its medical stainless steel composition, a material chosen for its mechanical resistance and compatibility with sterilization processes. This product is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH. Due to its design and the materials used, there is no defined maximum limit for processing cycles, although the instrument must be inspected before each use to detect any visible damage such as cracks, breaks, or defects on the cutting edges. Its regulatory classification as Class I confirms its status as a professional medical device.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer concerns hypersensitivity reactions. Contact with this medical stainless steel instrument may cause metal intolerance in some patients. If a hypersensitivity reaction or intolerance is triggered during the procedure, the procedure must be stopped immediately and necessary medical measures must be taken accordingly. It is therefore recommended to question the patient about their history of metal allergies before any use. Furthermore, the use of the instrument is strictly prohibited if it shows visible signs of wear or structural damage.
What maintenance and safety precautions must be followed?
Patient and practitioner safety relies on a strict reprocessing protocol. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. The manufacturer emphasizes that it is crucial to clean each product before proceeding with sterilization. A meticulous visual inspection is mandatory to identify any wear, cracks, or defects on the cutting edges; damaged products must never be used. Compatibility with other products used during the procedure must also be verified beforehand to ensure the smooth progress of the surgical act.
Who is the manufacturer and what standards are respected?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to the current regulations (MDR). Compliance with the rigorous manufacturing protocols of Helmut Zepf ensures consistent quality for manual dental surgery instruments. As a Class I device, it meets the safety and performance requirements defined for reusable surgical instruments. Professionals can refer to the instructions for use and safety provided by the manufacturer to ensure use in accordance with European medical standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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