Frontal Teeth Curette - Helmut Zepf (24.751.130) - Delynov
The Curette pour dents frontales - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.130.
- 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 frontal tooth curette (24.751.130)?
The Helmut Zepf frontal tooth curette, referenced under code 24.751.130, is a high-precision manual dental instrument designed for procedures on the anterior block. Manufactured by Helmut Zepf Medizintechnik GmbH, this curette is crafted from high-quality medical stainless steel to ensure optimal durability during periodontal and surgical care. This device belongs to the category of manual instruments (INSTRU) and is classified as a Class I medical device. Its specific structure allows for precise handling for the treatment of frontal tooth surfaces, meeting the requirements of dental surgeons and periodontists seeking reliable tools for their daily practice.
What are the clinical indications for this dental instrument?
This curette is specifically indicated as a manual dental instrument for the treatment of frontal teeth. Its use is reserved exclusively for qualified healthcare professionals. It is intended for use during scaling, root planing, or tissue cleaning procedures within the framework of periodontal care or oral surgery. The manufacturer Helmut Zepf specifies that the instrument must be inspected before each use to detect any visible damage, such as cracks, breaks, or defects on the cutting edges. The use of a damaged product is strictly prohibited to guarantee patient safety and the effectiveness of the clinical act.
What are the technical and maintenance characteristics of the device?
The Helmut Zepf curette (24.751.130) is manufactured from medical stainless steel, a material recognized for its mechanical resistance. Regarding maintenance, this device is delivered non-sterile. It is imperative to perform a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as before each subsequent use. The manufacturer indicates that due to the product design and the materials used, there is no defined maximum limit for the number of processing cycles that can be performed. The service life of the instrument depends on its physical condition: it must be discarded as soon as signs of wear or degradation of the sharp edges appear.
What are the contraindications for the use of this curette?
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, the use of this instrument is contraindicated if it shows visible signs of wear, cracks, or defects on the active parts, as this could compromise the safety of the care or injure periodontal tissues.
What are the precautions for use for healthcare professionals?
The use of the Helmut Zepf curette is strictly reserved for healthcare professionals. Before any intervention, it is crucial to verify the compatibility of this instrument with other products used. Thorough cleaning is mandatory before each sterilization to remove all residues. The practitioner must pay particular attention to the visual examination of the cutting edge: never use blunt instruments or those showing breaks. As the device is delivered non-sterile, compliance with reprocessing protocols (cleaning, disinfection, and sterilization) is the direct responsibility of the dental practice to prevent any risk of cross-contamination.
Who is the manufacturer and what standards are respected?
This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I instrument compliant with regulatory requirements for manual medical devices. The manufacturer ensures the traceability and quality of the medical stainless steel used. As a Helmut Zepf product, this instrument benefits from the expertise of an official manufacturer recognized in the dental sector. The safety and use instructions provided by Helmut Zepf Medizintechnik Gmbh must be scrupulously followed by professional users to guarantee the compliance and safety of the care provided to patients.
State of the art
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Specifications
| Manufacturer | Helmut Zepf |
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