Syndesmotome Chrompet FIG. 3 - Helmut Zepf (17.410.03)
Simplify your extractions with the Helmut Zepf Chrompet Syndesmotome
Optimize the luxation of roots and teeth during your extraction surgeries with this precision instrument designed for safe manual handling.
- Model: FIG. 3 (Left Curved).
- Use: Elevation of teeth and residual roots.
- Material: Biocompatible medical stainless steel.
- Safety: Class Ir device, delivered non-sterile for complete reprocessing.
The Syndesmotome Chrompet FIG. 3 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.410.03.
- 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 utilisé pour soulever les dents ou les racines dentairesrésiduelles lors de l'extraction d'une dent. 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 Syndesmotome Chrompet FIG. 3 from Helmut Zepf?
The Syndesmotome Chrompet FIG. 3, referenced under code 17.410.03 at Delynov, is a high-precision manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical-grade stainless steel, this robust tool is specifically developed for oral surgery interventions. Its ergonomic design allows for fluid handling during extraction procedures. As a Class I device, it meets the quality requirements for reusable surgical instruments. This particular model, often associated with the search terms syndesmotome chompret left curve, is an essential piece of instrumentation for practitioners demanding reliability and durability in their daily technical tray.
What are the clinical indications for the 17.410.03 syndesmotome?
The intended use for this Helmut Zepf instrument is strictly defined by the manufacturer for the dental field. It is primarily indicated for lifting teeth or residual dental roots during a dental extraction procedure. By facilitating the separation of the epithelial attachment and ligament fibers, it allows for easier luxation of the tooth, thereby minimizing trauma to the surrounding tissues. This instrument is exclusively reserved for qualified health professionals, such as dental surgeons and implantologists, performing simple or complex avulsions requiring fine and resistant stainless steel instrumentation.
What are the technical characteristics of this medical device?
The Syndesmotome Chrompet FIG. 3 (reference 17.410.03) is distinguished by its medical stainless steel composition, guaranteeing optimal corrosion resistance and increased longevity. Although exact dimensions are not specified, its morphology is adapted to difficult clinical access. It is a device delivered non-sterile by Helmut Zepf Medizintechnik GmbH. Before any use, it is imperative to perform a complete cleaning, disinfection, and sterilization cycle. The manufacturer specifies that due to the quality of the materials and design, there is no defined maximum limit for processing cycles, as long as the instrument does not show visible damage or wear on the cutting edges.
What are the contraindications and side effects related to use?
The main contraindication for using this instrument lies in the patient's known hypersensitivity to metals. Contact with medical stainless steel can trigger intolerance or hypersensitivity reactions 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 strictly prohibited if it shows visible damage such as cracks, breaks, or defects on the cutting edges. Misuse of its initial function of tooth lifting is also considered a contraindication by the manufacturer.
What maintenance and safety precautions must be followed?
To ensure patient safety and the longevity of the Helmut Zepf instrument, a strict reprocessing protocol is mandatory. All instruments must be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to meticulously inspect the syndesmotome before each intervention to detect any signs of wear or degradation. The use of damaged products is dangerous and prohibited. The sterilization process must follow standard recommendations for medical stainless steel. Finally, compatibility with other instruments used simultaneously during the surgical act must be verified beforehand by the practitioner.
Who is the manufacturer and what standards are met by this product?
The Syndesmotome Chrompet FIG. 3 is manufactured by 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 compliance of its products intended for healthcare professionals. As a Class I device, it complies with the essential safety and performance requirements defined for reusable manual surgical instruments. The instructions for use and safety provided by Helmut Zepf emphasize the importance of adhering to cleaning and sterilization protocols to maintain the compliance and effectiveness of the instrument over the long term.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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