Stone Burnisher 24.916.10
The Pierre à Repasser 24.916.10 is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- 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 Pierre à Repasser 24.916.10 from the Marque?
The Pierre à Repasser 24.916.10, marketed under the Marque, is a manual dental instrument designed for the maintenance of surgical devices. This product from the CONSO category is manufactured by Helmut Zepf Medizintechnik Gmbh. It is an essential tool for healthcare professionals in dental surgery and implantology, ensuring the maintenance of medical stainless steel instrumentation. In accordance with the manufacturer's instructions, this instrument must be handled with care to preserve the integrity of the cutting edges of the tools it is used to maintain. Its use is strictly reserved for qualified healthcare professionals.
What are the clinical indications for this instrument?
The primary indication for the Pierre à Repasser 24.916.10 from the Marque is the maintenance and rectification of manual dental instruments. Its use allows for the treatment of visible damage and wear such as defects on cutting edges, cracks, or minor breaks identified during pre-operative inspection. As a maintenance instrument for medical stainless steel devices, it contributes to the longevity of the instrument pool used in oral surgery. The manufacturer Helmut Zepf specifies that the condition of each product must be checked before use to ensure the safety of clinical procedures.
What are the technical and safety characteristics of this product?
The Pierre à Repasser 24.916.10 is classified as a Class I medical device. According to the specifications of the manufacturer Helmut Zepf, this instrument is delivered non-sterile. It is imperative to perform complete cleaning, disinfection, and sterilization before the first use, as well as before each subsequent use. Due to its design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, allowing for sustainable use in a clinical environment. Compatibility with other products in the surgical arsenal must be verified beforehand by the practitioner.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of Marque instruments concerns metal intolerance. Contact with the instrument, manufactured from medical stainless steel, may cause a hypersensitivity reaction in certain patients. If such a reaction occurs during the clinical procedure, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use the Pierre à Repasser 24.916.10 or any associated instrument if they show visible damage, cracks, or breaks, in order to avoid any risk of complication during the intervention.
What are the precautions for use and reprocessing?
The reprocessing of the Pierre à Repasser 24.916.10 from the Marque follows a rigorous protocol. All instruments must be cleaned, disinfected, and sterilized before each use. The manufacturer Helmut Zepf emphasizes the crucial importance of cleaning each product to remove any residue before sterilization. The user must inspect the tool to detect any visible wear on the cutting edges. If defects are identified, the instrument must no longer be used. The product's service life depends on the treatment cycles and the intended use, without a predefined maximum limit, subject to maintenance in accordance with the provided safety instructions.
Who is the manufacturer and what standards are respected?
The Pierre à Repasser 24.916.10 is manufactured by HELMUT ZEPF Medizintechnik Gmbh, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I and complies with regulatory requirements for manual dental instruments. Although the products are delivered non-sterile, they are designed to withstand standard hospital sterilization processes. The Marque guarantees that the medical stainless steel used meets biocompatibility standards, while warning professionals about the risks of metal hypersensitivity. This device is exclusively reserved for professional use within the framework of dental surgery and implantology.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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