CURETTE TIP, M4X0.5 - Helmut Zepf (24.751.204LD) - 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: 24.751.204LD.
- 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 24.751.204LD by Helmut Zepf, is a high-precision manual dental instrument. Designed by Helmut Zepf Medizintechnik GmbH, this tip is manufactured from superior quality medical stainless steel to ensure optimal performance during oral surgery interventions. This device belongs to the instrument category (INSTRU) and is classified as a Class I medical device. Its specific design with an M4X0.5 thread allows for precise integration onto compatible handles, thus offering a modular and durable solution for demanding practitioners.
What are the clinical indications for this instrument?
The CURETTE TIP M4X0.5 is indicated as a manual dental instrument for various procedures in dental and implant surgery. It is specifically designed to be handled by qualified healthcare professionals. Its primary use lies in the treatment of tissues and dental surfaces requiring fine and rigorous instrumentation. According to the instructions from the manufacturer Helmut Zepf Medizintechnik GmbH, the instrument must be carefully inspected before each use to detect any visible damage such as cracks, breaks, or defects on the cutting edges, in order to guarantee the safety and efficacy of the clinical procedure.
What are the technical characteristics of reference 24.751.204LD?
This curette tip is distinguished by its rigorous technical specifications, notably its M4X0.5 thread which ensures stable and secure fixation. Manufactured from medical stainless steel, it offers increased resistance to corrosion and a longevity adapted to frequent reprocessing cycles. The manufacturer specifies that due to the robust design of the product and the materials used, there is no defined maximum limit for the number of achievable processing cycles, although wear must be monitored. Helmut Zepf products are delivered non-sterile and require a complete preparation protocol before any commissioning.
What are the contraindications and side effects?
The use of the CURETTE TIP M4X0.5 presents specific contraindications related to the manufacturing materials. An undesirable side effect may occur in the form of metal intolerance in the patient, resulting from contact with the medical stainless steel. If a hypersensitivity reaction is triggered, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use products showing visible damage or wear, as this could compromise patient safety and the integrity of the surgical act.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use, as well as before each subsequent use. The cleaning process must be complete and rigorous to eliminate all residues. Before sterilization, the practitioner must verify compatibility with other products used. As the devices are delivered non-sterile, strict compliance with reprocessing protocols is essential. It is also crucial to check for the absence of cracks or defects on the cutting edges before each intervention. This device is exclusively reserved for healthcare professionals.
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 a Class I instrument, compliant with regulatory requirements for manual medical devices. Manufacturing is based on recognized expertise in the field of dental instrumentation, using medical stainless steel to ensure biocompatibility and durability. As a Class I device, it meets the safety standards imposed for reusable surgical instruments, subject to maintenance and sterilization in accordance with the instructions provided by the manufacturer.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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