White Excavator Fig. 19 - Helmut Zepf (24.733.19) - Delynov
The Excavateur Blanc Fig. 19 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.733.19.
- 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 Excavateur Blanc Fig. 19 - Helmut Zepf (24.733.19) - Delynov?
The Excavateur Blanc Fig. 19, bearing technical reference 24.733.19, is a high-precision manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. This Class I medical device is manufactured from medical stainless steel, ensuring robustness suited to the demands of clinical practice. As a manual instrument, it is specifically developed for dental and oral surgery interventions. This product is delivered non-sterile by the manufacturer, requiring rigorous processing before its first use in the practice. Its ergonomic design meets the quality standards of the Helmut Zepf brand, recognized in the field of odontological instrumentation.
What are the clinical indications for this instrument?
The intended use of this Helmut Zepf manual dental instrument is strictly reserved for qualified healthcare professionals. It is indicated for dental care procedures requiring the use of an excavator, particularly for the removal of softened dentinal tissue or the cleaning of cavities. Its application falls within the scope of routine oral and dental surgery interventions. The practitioner must imperatively check the integrity of the instrument before each act, ensuring the absence of visible damage such as cracks or defects on the cutting edges, to guarantee optimal efficiency and patient safety.
What are the technical characteristics of the excavator 24.733.19?
The Helmut Zepf Fig. 19 excavator is distinguished by its manufacture in medical stainless steel, a material chosen for its resistance and compatibility with sterilization processes. This device belongs to the category of reusable consumables (CONSO) of Class I. Its technical design does not allow for a defined maximum limit of treatment cycles, as the lifespan depends directly on the maintenance and wear observed by the professional. It is crucial to note that this instrument must be cleaned, disinfected, and sterilized before the first use and after each subsequent use to maintain its functional properties and safety level.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this medical stainless steel excavator is metal intolerance or hypersensitivity in the patient. Contact with the instrument may trigger an allergic reaction. In the event of such a hypersensitivity reaction during the procedure, the manufacturer Helmut Zepf Medizintechnik GmbH recommends immediately stopping the intervention and taking the necessary medical measures. Additionally, the use of the instrument is formally prohibited if it shows visible signs of wear, breaks, or damaged cutting edges, as this could compromise the safety of the care.
What are the maintenance and reprocessing precautions?
All instruments supplied by Helmut Zepf Medizintechnik GmbH are delivered non-sterile. The safety protocol requires complete cleaning, disinfection, and sterilization before the first commissioning and between each patient. It is essential to inspect the excavator for any cracks or defects before any use. Due to the nature of the materials used and the design of the device, there is no predefined limit on the number of reprocessing cycles. However, compatibility with other cleaning and sterilization products must be verified beforehand by the healthcare professional responsible for the device.
Who is the manufacturer and what standards are met?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I in accordance with current regulations (MDR). The manufacturer ensures the traceability and compliance of the instrument as a manual dental instrument intended exclusively for healthcare professionals. Although the specific CE marking is not detailed in the source data, the product meets the requirements for Class I devices in medical stainless steel. Each unit is identified by the reference 24.733.19, guaranteeing the German origin and manufacturing quality.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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