Spare Jaws for Forceps - Helmut Zepf (19.270.50) - Delynov
The Mors de rechange pour pince - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.270.50.
- 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 are the replacement jaws for Helmut Zepf pliers (19.270.50)?
The replacement jaws for pliers, referenced under code 19.270.50, are interchangeable components designed by Helmut Zepf Medizintechnik GmbH. Manufactured from high-quality medical stainless steel, these accessories are intended to be mounted on specific manual dental instruments. This device belongs to the GBR (Guided Bone Regeneration) category and is part of a sustainability approach for surgical instruments. As a Class I instrument, it meets the regulatory requirements for use in a clinical setting. Its medical steel design ensures the robustness necessary for precision interventions while allowing for rigorous maintenance. These jaws maintain the functional performance of the original pliers without requiring the complete replacement of the instrument.
What are the clinical indications for this device?
The intended use for these Helmut Zepf replacement jaws is as a manual dental instrument intended for oral surgery and implantology interventions. They are specifically indicated for procedures requiring precise manipulation of tissues or materials within the framework of guided bone regeneration (GBR). This device is exclusively reserved for qualified healthcare professionals. Its use occurs in a surgical context where the reliability of the grip and the quality of the material are essential for the success of the operative act. The manufacturer specifies that the instrument must be checked before each use to detect any visible damage, such as cracks or defects on the edges, in order to guarantee patient safety and clinical efficacy.
What are the technical characteristics of these replacement jaws?
These replacement jaws, bearing technical reference 19.270.50, are characterized by their medical stainless steel composition, a material chosen for its resistance and compatibility with sterilization protocols. They are delivered non-sterile by Helmut Zepf Medizintechnik GmbH. The product design and the materials used do not allow for the definition of a strict maximum limit of processing cycles, as the service life depends on visible wear and the care taken during reprocessing. It is imperative to verify compatibility with other products and instruments before any intervention. The absence of structural defects, such as breakages or premature wear, must be systematically checked by the practitioner before clinical implementation.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer concerns metal intolerance. Contact with this medical stainless steel instrument may lead to undesirable side effects or a hypersensitivity reaction in certain sensitive patients. If such a reaction occurs during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. Furthermore, it is strictly forbidden to use products showing visible damage or wear, such as cracks or defective cutting edges. Compliance with these safety instructions is crucial to prevent any risk of intraoperative complication related to the physical integrity of the instrument.
What are the maintenance and sterilization precautions?
Like all Helmut Zepf instruments, these replacement jaws must imperatively be cleaned, disinfected, and sterilized before their first use, as well as before each subsequent use. The reprocessing process must be complete to guarantee asepsis. The manufacturer insists on the importance of cleaning each product individually before use. Being delivered non-sterile, the sterilization cycle is a mandatory step under the responsibility of the healthcare professional. It is also appropriate to monitor for signs of wear, as the use of damaged products is prohibited. Although no maximum limit of cycles is defined by the design, replacement must be carried out as soon as functional or aesthetic alterations are detected on the steel.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to current regulations. The manufacturer ensures the compliance of its manual instruments with safety and performance requirements for professional dental use. Helmut Zepf's rigorous manufacturing protocols guarantee the use of medical stainless steel adapted to the constraints of oral surgery. Healthcare professionals must refer to the manufacturer's instructions for cleaning and sterilization in order to maintain device compliance throughout its useful life. This equipment is strictly reserved for use by qualified medical personnel.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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