Skip to Content

CURETTE TIP. M4X0.5. - Helmut Zepf (24.751.114C) - Delynov

https://www.delynov.fr/web/image/product.template/9636/image_1920?unique=a854c9c

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: 24.751.114C.
  • 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.

31.60 € 31.6 EUR 31.60 € Tax Included

31.60 € Tax Included

(31.60 € / Units)
  • Manufacturer

This combination does not exist.

Instrument

What is the Helmut Zepf CURETTE TIP M4X0.5?

The CURETTE TIP M4X0.5, referenced under code 24.751.114C, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from high-quality medical stainless steel, ensuring robustness adapted to the requirements of dental surgery. As an instrument in the INSTRU category, it is an interchangeable tip equipped with a specific M4X0.5 thread. This product is delivered non-sterile by Helmut Zepf and requires a rigorous preparation protocol before any clinical intervention. Its design allows for precise integration onto compatible handles for curettage and periodontal or surgical cleaning procedures.

What are the clinical indications for this Helmut Zepf instrument?

This manual dental instrument is specifically indicated for oral and dental surgery interventions requiring precise curettage of tissues or root surfaces. The manufacturer Helmut Zepf specifies that the use of this curette tip is exclusively reserved for qualified healthcare professionals. It is used for the removal of tartar deposits, cleaning of sockets, or tissue debridement during implantology or periodontology protocols. The primary indication is based on manual handling for optimal tactile control during the excision of pathological tissues or debris, thus ensuring adequate preparation of the surgical site before subsequent steps of care or reconstruction.

What are the technical characteristics of the curette tip 24.751.114C?

The Helmut Zepf curette tip is distinguished by its M4X0.5 technical thread, ensuring stable and secure fixation on compatible instrument supports. Manufactured from medical stainless steel, it offers high mechanical resistance essential for the forces applied during curettage. This device belongs to Class I of medical devices according to current regulations. An essential characteristic lies in its durability: due to the materials used and its design, there is no defined maximum limit for processing cycles, although the user must imperatively check for the absence of visible damage, such as cracks or defects on the cutting edges, before each use.

What are the contraindications and side effects for the use of this instrument?

The main contraindication to the use of this medical stainless steel instrument is metal intolerance or known hypersensitivity of the patient to this material. Contact with the instrument may trigger a hypersensitivity reaction in certain subjects. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is formally contraindicated if it shows visible signs of wear, breakage, or blunt cutting edges, as this could compromise patient safety and the effectiveness of the surgical act.

What are the maintenance and sterilization precautions?

As Helmut Zepf Medizintechnik GmbH products are delivered non-sterile, a strict reprocessing protocol is mandatory. Before the first use, as well as before each subsequent use, the instrument must be fully cleaned, disinfected, and sterilized. It is crucial to proceed with thorough cleaning to remove all organic residue. The user must also systematically check the physical condition of the tip (absence of cracks or deformations). Compatibility with other products and instruments used during the procedure must be verified beforehand. Being a non-resorbable instrument, its maintenance relies on the quality of the sterilization cycle to guarantee the asepsis of the surgical field.

Who is the manufacturer and what standards are met by this device?

The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I, in accordance with regulatory requirements relating to manual dental instruments. The manufacturer insists that the use of this instrument is strictly reserved for healthcare professionals. Compliance with the safety and usage instructions provided by Helmut Zepf is imperative to guarantee the conformity of care. Although specific CE marking is not detailed in the source data, the Class I classification confirms its status as a regulated medical device within the European Union for professional dental use.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
Tags
Tags
Instrument