Axial Instrument - Helmut Zepf (26.200.17) - Delynov
The Instrument axial - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 26.200.17.
- 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 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 axial instrument (26.200.17)?
The axial instrument with reference 26.200.17 is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device is manufactured from medical grade stainless steel, ensuring robustness adapted to the requirements of dental surgery. It is presented as an indispensable precision tool for practitioners. In accordance with hygiene protocols, this instrument is delivered non-sterile by Helmut Zepf and requires complete processing before its first use in the practice or operating room.
What are the clinical indications for this dental instrument?
This manual instrument is specifically indicated for dental surgery procedures. Its intended purpose is to assist the healthcare professional in daily interventions in odontology or implantology. As a manual dental instrument, it is reserved exclusively for qualified healthcare professionals. Its use must be preceded by a meticulous check of the instrument's condition, particularly the absence of visible damage such as cracks, breaks, or defects on the cutting edges, in order to guarantee patient safety during the surgical act.
What are the technical characteristics of the axial instrument?
The Helmut Zepf axial instrument (reference 26.200.17) is distinguished by its medical stainless steel composition, a material chosen for its durability and resistance to sterilization cycles. Due to its design and the materials used, the manufacturer specifies that there is no defined maximum limit for the number of processing cycles achievable, as long as the physical integrity of the tool is preserved. It belongs to the INSTRU category and is regulatory classified as Class I. Each product must be inspected before use to detect any signs of premature wear.
What are the contraindications for the use of this device?
The main contraindication related to the use of this medical stainless steel instrument is metal intolerance in the patient. A hypersensitivity reaction may be triggered upon contact with the instrument. If such a reaction occurs, the surgical procedure must be immediately interrupted and necessary medical measures must be taken. It is also formally contraindicated to use the instrument if it shows visible signs of wear, cracks, or if the cutting edges are damaged, as this could compromise the safety of the care.
What are the maintenance and reprocessing precautions?
The reprocessing of this Helmut Zepf manual instrument follows strict safety instructions. All instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. The manufacturer emphasizes the vital importance of complete cleaning before each sterilization cycle. Before any intervention, the practitioner must check compatibility with other products used. The use of damaged or worn products is strictly prohibited to avoid any risk of breakage or intraoperative complication.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This official manufacturer guarantees a Class I medical device compliant with regulatory requirements for manual dental instruments. The product is identified under reference code 26.200.17 at Delynov. As a Class I device, it meets the safety and performance standards applicable to reusable medical stainless steel instruments, subject to strict compliance with the cleaning and sterilization protocols issued by Helmut Zepf.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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