Composite Spatula - Helmut Zepf (24.751.327TI) - Delynov
The SPATULE POUR COMPOSITE. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.327TI.
- 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 composite spatula (24.751.327TI)?
The Helmut Zepf composite spatula, referenced under code 24.751.327TI, is a high-precision manual dental instrument designed for the manipulation of restorative materials. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument belongs to the consumables (CONSO) category and is classified as a Class I device according to current regulations. Its robust structure and ergonomic design allow for smooth and precise application of composites during restorative dentistry procedures. This product is delivered non-sterile and requires rigorous preparation before any clinical intervention.
What are the clinical indications for this manual instrument?
This manual dental instrument is specifically indicated for dental restoration procedures involving the use of composites. As a precision tool, it facilitates the modeling and application of filling materials. Its use is strictly reserved for qualified healthcare professionals working in dental surgery or general dentistry. The manufacturer specifies that the instrument must be systematically checked before use to detect any visible damage, such as cracks or defects on the cutting edges, in order to guarantee patient safety and the effectiveness of the clinical procedure.
What are the technical characteristics of the 24.751.327TI spatula?
The Helmut Zepf composite spatula is distinguished by its medical stainless steel composition, a material chosen for its durability and resistance to repeated treatment cycles. Although there is no defined maximum limit for the number of reprocessing cycles due to the quality of the materials used, the lifespan of the instrument depends on its maintenance. It is imperative to check for visible wear before each use. This manual device is designed to offer optimal maneuverability during the shaping of dental materials, meeting the technical requirements of the most demanding practitioners.
What are the contraindications for the use of this instrument?
The main contraindication 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 procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, it is formally prohibited to use damaged or worn products, presenting for example breaks or structural defects, as this could compromise the safety of the care and the integrity of the patient's tissues.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use, as well as before each subsequent use. The reprocessing process must be complete and rigorous. It is essential to check compatibility with other products used simultaneously. As the device is delivered non-sterile, compliance with cleaning and sterilization protocols is a sine qua non condition for its clinical use. The manufacturer emphasizes the importance of cleaning each product before use to eliminate any residue and guarantee perfect asepsis in the dental office.
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 medical device, compliant with regulatory requirements relating to manual dental instruments. The manufacturer ensures the traceability and quality of its products through rigorous manufacturing standards. As a Class I device, it meets the safety and performance standards for professional use in a medical environment. Practitioners can refer to the instructions for use and safety provided to ensure use in accordance with the manufacturer's guidelines.
State of the art
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Specifications
| Manufacturer | Helmut Zepf |
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