Pointed Curette M4X0.5 - Helmut Zepf (24.751.123L)
The Curette Pointée 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: 24.751.123L.
- 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 Pointed Curette M4X0.5 - Helmut Zepf (24.751.123L)?
The Pointed Curette M4X0.5, with reference 24.751.123L, is a high-precision manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. This device is manufactured from high-quality medical stainless steel, ensuring robustness suited to the demands of dental surgery. As an instrument in the INSTRU category, it is integrated into manual care protocols requiring fine and reliable instrumentation. This product is delivered non-sterile and requires a complete preparation cycle before its first use. Its specific design allows for precise manipulation during clinical interventions, meeting the high standards of the Helmut Zepf brand in terms of surgical instrumentation.
What are the clinical indications for this dental instrument?
The Pointed Curette M4X0.5 is indicated as a manual dental instrument for oral care procedures. Its use is strictly reserved for qualified healthcare professionals. It is primarily used during interventions requiring precise manual action on dental tissues or structures. The manufacturer Helmut Zepf specifies that the instrument must be inspected before each use to detect any visible damage, such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn product is formally prohibited to guarantee patient safety and the effectiveness of the surgical act.
What are the technical characteristics of the 24.751.123L curette?
Technically, this instrument is distinguished by its M4X0.5 thread and its specific reference 24.751.123L. Manufactured from medical stainless steel, it offers optimal resistance to repeated treatment cycles. Helmut Zepf emphasizes that due to the product design and materials used, there is no defined maximum limit for the number of achievable treatment cycles, although wear must be visually monitored by the practitioner. This device belongs to Class I of medical devices. It must imperatively be cleaned, disinfected, and sterilized before the first use, as well as between each patient, to maintain its technical performance and structural integrity.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns metal intolerance. Contact with this medical stainless steel instrument may cause a hypersensitivity reaction in certain sensitive patients. If such an allergic reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of this instrument is contraindicated if it shows visible signs of wear, defects on the edges, or cracks, as this could compromise treatment safety and patient health.
What are the maintenance and sterilization precautions?
The reprocessing protocol is crucial for the longevity of this Helmut Zepf instrument. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to perform complete cleaning to remove all residues before the sterilization phase. The practitioner must verify compatibility with other products used simultaneously. As the device is delivered non-sterile, rigorous compliance with the manufacturer's instructions for use and safety is mandatory. Careful examination of the medical stainless steel condition ensures the absence of damage before any insertion into the mouth.
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 is classified as Class I according to current regulations. The manufacturer ensures the traceability and quality of its manual instruments intended for healthcare professionals. Although the specific CE marking is not detailed in the provided sources, the product meets the safety requirements for manual dental instruments in stainless steel. Each instrument is designed to withstand multiple treatment cycles, subject to maintenance in accordance with Helmut Zepf technical directives.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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