Interchangeable Probe Tips - Helmut Zepf (24.751.108) - Delynov
The Pointe de sonde interchangeable - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.108.
- 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 interchangeable probe tip (24.751.108)?
The Helmut Zepf interchangeable probe tip, referenced under code 24.751.108, is a manual dental instrument designed for use during oral and dental surgery procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, this tip is made of high-quality medical stainless steel to ensure optimal performance during clinical examination. This device belongs to the consumables category (CONSO) and is classified as a Class I medical device. Its interchangeable design allows for flexibility of use on the brand's compatible handles, ensuring easy maintenance and increased durability of the equipment within the dental practice.
What are the clinical indications for this manual dental instrument?
This instrument is specifically indicated for use as a manual dental instrument within the framework of various clinical procedures. It is intended for healthcare professionals, such as dental surgeons and implantologists, for exploration and diagnosis during dental care. Due to its medical stainless steel nature, it offers the precision necessary for routine examinations or more complex oral surgery interventions. It is imperative that the user verifies the integrity of the instrument before each use, ensuring the absence of visible damage, cracks, or defects on the cutting edges to guarantee patient safety.
What are the technical characteristics of reference 24.751.108?
The Helmut Zepf 24.751.108 probe tip is distinguished by its rigorous manufacture in medical stainless steel, a material chosen for its resistance and compatibility with sterilization processes. This device is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use, as well as after each subsequent use. Due to its design and the materials used, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that there is no defined maximum limit for processing cycles, as long as the instrument does not show signs of wear or structural damage compromising its safe use.
What are the contraindications for the use of this probe tip?
The main contraindication related to the use of this instrument is metal intolerance in the patient. Contact with medical stainless steel can trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, the healthcare professional must immediately stop the intervention and take the necessary medical measures. Furthermore, it is formally contraindicated to use damaged or worn products, presenting, for example, breaks or defects on the edges. The use of this instrument is strictly reserved for qualified healthcare professionals mastering hygiene protocols and the use of manual dental devices.
What are the maintenance and reprocessing precautions for the device?
The reprocessing of the Helmut Zepf probe tip is a critical step for safety. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer emphasizes the importance of checking compatibility with other products before use. Before each intervention, the practitioner must visually inspect the tip to detect any signs of wear, cracks, or defects. Due to the robustness of medical stainless steel, the number of achievable processing cycles depends on the physical condition of the instrument. Any product showing visible damage must be immediately removed from the clinical circuit to avoid any risk of breakage or injury.
Who is the manufacturer and what standards are met by this product?
This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device (Class Ir according to certain reprocessing specifications), compliant with regulatory requirements for manual dental instruments. The manufacturer ensures the traceability and quality of the medical stainless steel used. In accordance with European Medical Device Regulations (MDR), the use of this product is reserved exclusively for healthcare professionals. Compliance with the cleaning and sterilization protocols recommended by Helmut Zepf is essential to maintain the device's conformity and ensure patient safety throughout its useful life.
State of the art
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Specifications
| Manufacturer | Helmut Zepf |
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