Curette Tip, M4X0.5 - Helmut Zepf (24.751.105G)
The POINTE DE CURETTE. M4X0.5. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.105G.
- 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 M4X0.5 curette tip?
The M4X0.5 curette tip, referenced under code 24.751.105G by Helmut Zepf, is a high-precision manual dental instrument. Designed by Helmut Zepf Medizintechnik GmbH, this part is manufactured from medical stainless steel, a material selected for its robustness and compatibility with the requirements of the surgical environment. This device belongs to the category of instruments (INSTRU) and is classified as a Class I medical device. It is specifically developed to be integrated into a manual dental instrumentation system, offering a durable solution for demanding practitioners. Like all products of the brand, this tip is delivered non-sterile and requires a complete preparation protocol before any clinical use.
What are the clinical indications for this instrument?
This Helmut Zepf curette tip is indicated for use as a manual dental instrument during oral care procedures. Its use is strictly reserved for qualified healthcare professionals. It is primarily intended for interventions requiring precise instrumentation for the treatment of dental or periodontal surfaces. The main indication is based on manual manipulation during curettage or specialized cleaning phases. The manufacturer emphasizes the importance of checking the integrity of the instrument before each act: the presence of visible damage, cracks, breaks, or defects on the cutting edges must lead to the immediate disposal of the product to guarantee patient safety and the effectiveness of the surgical gesture.
What are the technical characteristics of the 24.751.105G tip?
The Helmut Zepf curette tip is distinguished by its M4X0.5 thread, allowing a precise and stable connection with compatible handles. Manufactured from medical stainless steel, it benefits from a design optimized for reprocessing. Although the manufacturer does not indicate a defined maximum limit of processing cycles due to the quality of the materials used, the service life of the instrument depends on usage and compliance with maintenance protocols. It is imperative to check the wear of the cutting edges before each intervention. This Class I device must be systematically cleaned, disinfected, and sterilized before its first use, and then after each subsequent use, to maintain its technical performance and safety of use.
What are the contraindications for the use of this instrument?
The main contraindication to the use of this Helmut Zepf instrument lies in the patient's known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact may trigger a hypersensitivity reaction in certain sensitive subjects. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that the intervention must be stopped immediately and that the necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible signs of wear, cracks, or damaged cutting edges, as this could compromise the safety of the care or injure surrounding tissues.
What are the maintenance and sterilization precautions?
Helmut Zepf products are delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before the first use and between each patient. It is crucial to carefully clean each product to remove any residue before the sterilization process. The manufacturer recommends a rigorous inspection to detect any visible damage (cracks, breaks). Due to the design and materials of the curette tip, the number of reprocessing cycles is not arbitrarily limited, but must be determined by the practitioner based on the observed wear. The use of damaged or worn instruments is strictly prohibited. Compatibility with other devices must also be verified beforehand.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device complies with the regulations in force for Class I (Class Ir according to certain reprocessing mentions). As a manual dental instrument, it meets the safety and performance requirements defined by the manufacturer for professional use in dental offices or hospital environments. Traceability is ensured by the product reference 24.751.105G. Compliance with the cleaning and sterilization protocols recommended by Helmut Zepf is essential to guarantee the conformity of the device throughout its useful life, thus ensuring a clinical practice that is safe and compliant with medical standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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