Curette Tip M4X0.5 - Helmut Zepf (24.751.113C)
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: 24.751.113C.
- 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 24.751.113C, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device is manufactured from medical-grade stainless steel, guaranteeing robustness adapted to the requirements of dental instrumentation. This product belongs to the instrument category (INSTRU) and is presented as an interchangeable tip intended to be mounted on a compatible handle. Its medical stainless steel design ensures optimal longevity, although the absence of a maximum limit for processing cycles is correlated with rigorous maintenance and the absence of visible wear. This device is exclusively reserved for use by qualified healthcare professionals.
What are the clinical indications for this Helmut Zepf instrument?
The primary indication for this Helmut Zepf manual dental instrument is periodontal and surgical treatment in the oral environment. As a curette, it is used by dental surgeons and implantologists for cleaning, scaling, or root planing, depending on the specific configuration of the tip. The intended purpose is to provide a precision tool for manual interventions requiring fine manipulation of tissues or dental surfaces. It is imperative that the practitioner verifies the compatibility of this tip with other products and handles used before any intervention. The instrument is delivered non-sterile and requires a complete preparation protocol before its clinical commissioning.
What are the technical characteristics of the 24.751.113C tip?
The Helmut Zepf curette tip (reference 24.751.113C) is distinguished by its M4X0.5 connection, allowing precise attachment to suitable instrument-holding handles. Manufactured from medical stainless steel, it offers high mechanical resistance for dental surgery procedures. Due to its design and the materials used, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that it is not possible to define a maximum limit for reprocessing cycles. The service life of the instrument depends directly on maintenance and visual inspection before each use. Any sign of visible damage, such as cracks, breaks, or defects on the cutting edges, must result in the immediate disposal of the tip.
What are the contraindications for the use of this stainless steel instrument?
The main contraindication to the use of this Helmut Zepf instrument lies in the patient's known hypersensitivity to metals. Contact with medical stainless steel can trigger an intolerance or hypersensitivity reaction in certain subjects. If such a reaction occurs during the surgical procedure, the procedure must be immediately stopped and necessary medical measures must be taken accordingly. Furthermore, the use of the instrument is strictly prohibited if it shows signs of wear, deformation, or blunt cutting edges, as this could compromise patient safety and the effectiveness of the clinical gesture. Compliance with cleaning and sterilization protocols is mandatory to avoid any infectious risk.
What are the maintenance and sterilization precautions?
Helmut Zepf products are delivered non-sterile and must imperatively follow a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as before each subsequent reuse. It is crucial to clean each product individually to remove any residue. Before each use, the professional must meticulously inspect the tip to detect any visible damage such as cracks or defects on the sharp parts. The use of damaged or worn products is formally prohibited. Reprocessing must be carried out according to the standards in force for Class I medical devices, taking into account that the number of achievable cycles depends on the physical state of the steel and the quality of the maintenance performed by the practice.
Who is the manufacturer and what standards are respected?
The curette tip is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to the regulations in force. The manufacturer imposes strict safety instructions: the instrument is reserved exclusively for healthcare professionals. Although specific CE marking is not detailed in the source data, the product meets the manufacturing requirements for manual dental instruments in medical stainless steel. Traceability is ensured by technical reference 24.751.113C. Compliance with cleaning, disinfection, and sterilization protocols (MDR) is the responsibility of the practitioner to ensure compliance and safety during dental care.
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Specifications
| Manufacturer | Helmut Zepf |
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