Prichard Periosteal Elevator - Helmut Zepf (24.751.126) - Delynov
The Rugine pour Prichard - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.126.
- 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 Prichard Periosteal Elevator Helmut Zepf (24.751.126)?
The Prichard Periosteal Elevator, referenced under code 24.751.126 by Helmut Zepf, is a high-precision manual dental instrument designed for oral surgery interventions. Manufactured from superior quality medical stainless steel, this tool is distinguished by its robustness and durability. As a Class I device, it meets the regulatory requirements for reusable surgical instruments. This product is delivered non-sterile by Helmut Zepf Medizintechnik GmbH, which requires a strict preparation protocol before any clinical use. Its ergonomic design allows for easy handling by the practitioner during delicate soft tissue elevation or manipulation procedures.
What are the clinical indications for this instrument?
The Prichard Periosteal Elevator is specifically indicated as a manual dental instrument for oral surgery procedures. Its primary role is to assist the dental surgeon or implantologist in flap management and work on periodontal tissues. It is used for the precise elevation of the periosteum and tissue manipulation during various surgical interventions. This device is exclusively reserved for qualified healthcare professionals. The use of this Helmut Zepf instrument guarantees a rigorous approach during the preparatory or corrective phases in implantology and periodontology, thus ensuring an intervention compliant with current clinical standards.
What are the technical characteristics of the 24.751.126 periosteal elevator?
Technically, the Prichard Periosteal Elevator Helmut Zepf is developed from a medical stainless steel selected for its mechanical resistance and biological compatibility. Although no maximum limit for processing cycles can be defined due to the nature of the materials and design, the longevity of the instrument depends on its maintenance. It is imperative to inspect the tool 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 instrument is strictly prohibited to guarantee patient safety and the effectiveness of the surgical act.
What are the contraindications for the use of this device?
The main contraindication for the use of this Helmut Zepf instrument lies in hypersensitivity or intolerance to metals in the patient. Contact with medical stainless steel can trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial for the practitioner to check the patient's allergic history before any use. Additionally, use is contraindicated if the instrument shows signs of wear or structural degradation compromising its integrity.
What are the maintenance and sterilization precautions?
As the Prichard Periosteal Elevator is delivered non-sterile, it must imperatively follow a complete reprocessing cycle before the first use and after each subsequent use. This protocol mandatory includes cleaning, disinfection, and sterilization steps. The manufacturer Helmut Zepf Medizintechnik GmbH emphasizes the importance of cleaning each product meticulously before submitting it to sterilization. The practitioner must also verify the compatibility of this instrument with other products used during the procedure. Rigorous maintenance is the guarantor of aseptic safety and the long-term preservation of the functional properties of the stainless steel.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This manufacturer is recognized for its expertise in the production of precision dental instruments. The Prichard Periosteal Elevator (24.751.126) is classified as a Class I medical device, in accordance with current regulations. Compliance with the cleaning and sterilization protocols recommended by the manufacturer ensures compliance with safety requirements for reusable devices. As a product intended exclusively for healthcare professionals, it benefits from German industrial rigor regarding manual medical devices.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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