Curette Tip, M4x0.5 - Helmut Zepf (24.751.204R) - Delynov
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: 24.751.204R.
- 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 CURETTE TIP M4X0.5?
The CURETTE TIP M4X0.5, referenced under code 24.751.204R by Helmut Zepf, is a high-precision manual dental instrument. Designed by Helmut Zepf Medizintechnik GmbH, this interchangeable tip is manufactured from high-quality medical stainless steel to guarantee optimal durability during oral surgery procedures. This device belongs to the instrument category (INSTRU) and is distinguished by its specific M4X0.5 threading, allowing for rigorous adaptation to compatible handles. As a Class I medical device, it meets safety requirements for routine dental surgical acts, offering practitioners a reliable tool for the treatment of dental and periodontal surfaces.
What are the clinical indications for this Helmut Zepf instrument?
This manual dental instrument is specifically indicated for curettage and tissue cleaning procedures within the framework of dental surgery and implantology. Its intended purpose is to allow the healthcare professional to perform precise movements on dental structures. The use of the Helmut Zepf curette tip is reserved exclusively for qualified healthcare professionals. It is particularly suitable for interventions requiring fine instrumentation for the treatment of periodontitis or the preparation of surgical sites. The manufacturer emphasizes the importance of verifying the suitability of this instrument with other products used during the clinical procedure.
What are the technical characteristics of the 24.751.204R curette tip?
The Helmut Zepf curette tip (ref. 24.751.204R) is characterized by its medical stainless steel design, a material chosen for its resistance and compatibility with sterilization processes. Its main technical specification lies in its M4X0.5 threading, ensuring a stable and secure connection with the handle. Before any use, the practitioner must imperatively inspect the instrument to detect any potential damage or visible wear, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to guarantee patient safety and the effectiveness of the surgical act.
What are the contraindications for the use of this device?
The main contraindication related 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 an allergic reaction or intolerance occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken accordingly. It is the practitioner's responsibility to check the patient's history of metal allergies before any manipulation. Furthermore, the instrument must not be used if it shows marked signs of wear or structural defects compromising its integrity.
What are the maintenance and sterilization precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. It is imperative to clean, disinfect, and completely sterilize each instrument before the first use, as well as before each subsequent use. Reprocessing must follow a strict protocol: thorough cleaning to remove all residue, followed by sterilization in accordance with hospital standards. Due to the robust design and materials used, there is no defined maximum limit for treatment cycles, as long as the instrument does not show visible damage. Compatibility with other cleaning and disinfection products must be verified beforehand by the dental practice.
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 product is classified as a Class I medical device according to current regulations. The manufacturer imposes strict safety instructions, reminding that the use of this instrument is exclusively reserved for healthcare professionals. Compliance with cleaning and sterilization protocols is a sine qua non condition for maintaining the conformity and safety of the device. Each Helmut Zepf curette tip is subject to rigorous quality controls to meet the requirements of the most demanding dental surgeons and implantologists.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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