FRACTURE BENDING FRACTURE WIRE SPLINTS - Helmut Zepf
The Helmut Zepf suture by Helmut Zepf Medizintechnik GmbH is a monofilament synthetic medical device for oral and implant surgery.
- Material: x 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..
- Packaging: Box of 24 single-use sterile sutures.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
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 pliable fracture wire splint (41.907.02S)?
The pliable fracture wire splint for fractures, referenced under code 41.907.02S by Delynov, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This medical device is manufactured from medical-grade stainless steel, ensuring robustness adapted to the requirements of maxillofacial and dental surgery. As a manual instrument, this splint is specifically developed for stabilization and support during the treatment of fractures. It belongs to the category of suture and retention instruments. In accordance with regulatory requirements, this product is classified as a Class I device, highlighting its supervised professional use in the oral health sector.
What are the clinical indications for this instrument?
The Helmut Zepf pliable fracture wire splint is indicated as a manual dental instrument for the management of fractures. Its intended purpose is to assist the practitioner during bone or dental stabilization procedures requiring a malleable splint. It is primarily used by dental surgeons, oral surgeons, and implantologists in contexts of dento-alveolar traumatology. This device allows for precise adaptation to the patient's anatomy thanks to its pliable design, thus facilitating the placement of effective retention during the healing phase. Its use is strictly reserved for qualified healthcare professionals mastering fracture reduction and fixation techniques in the oral sphere.
What are the technical characteristics of the 41.907.02S splint?
This fracture wire splint is distinguished by its medical stainless steel composition, a material chosen for its mechanical properties and relative biocompatibility. The technical reference 41.907.02S designates a pliable model, offering the flexibility necessary to fit dental arches or fractured bone structures. The product is delivered non-sterile by Helmut Zepf Medizintechnik GmbH, which requires a strict preparation protocol before any intervention. Due to its design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, although the condition of the instrument must be rigorously checked by the practitioner before each use to ensure the integrity of the device.
What are the contraindications for the use of this device?
The main contraindication related to the use of this medical stainless steel splint is metal intolerance in the patient. A hypersensitivity reaction or intolerance may result from direct contact with the instrument. The manufacturer specifies that if such a reaction is triggered, the procedure must be immediately stopped and the necessary medical measures must be taken accordingly. It is therefore crucial for the healthcare professional to evaluate the patient's allergic history before the intervention. Furthermore, the use of the instrument is contraindicated if it presents visible damage such as cracks, breaks, or defects on the edges, in order to avoid any additional traumatic risk.
What are the precautions for use and maintenance?
The Helmut Zepf fracture wire splint requires a rigorous maintenance protocol. All instruments must be cleaned, disinfected, and sterilized before the first use, as well as before each subsequent use. Complete cleaning is a critical step to ensure patient safety. The practitioner must carefully inspect the product for any visible wear, such as cracks or breaks, before the surgical act. It is strictly forbidden to use damaged or worn products. As the device is delivered non-sterile, compliance with reprocessing cycles in accordance with the manufacturer's instructions is mandatory. Compatibility with other products used during surgery must also be verified beforehand.
Who is the manufacturer and what standards are respected?
The fracture wire splint is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device complies with the regulations in force for manual dental instruments and is registered under Class I. The manufacturer ensures the traceability and quality of materials through the use of medical stainless steel. Compliance with cleaning, disinfection, and sterilization instructions is essential to maintain the product's conformity during its clinical use. As a Class I device, it meets the safety and performance requirements defined for non-invasive or invasive surgical instruments for temporary use, subject to exclusive handling by healthcare professionals.
State of the art
Modern synthetic sutures - absorbable or non-absorbable - are central to wound healing in oral surgery. Recent advances focus on reducing post-operative infections.
Specifications
| Manufacturer | Helmut Zepf |
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