TISSUE FORCEPS 1X2 - Helmut Zepf (22.408.20) - Delynov
Product features
The PINCE A GRIFFES 1X2. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.408.20.
- 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 chirurgical permettant de maintenir/saisir de manière atraumatique/chirurgicale des tissus, ou de maintenir/retirer des corps étrangers, des sutures ou des écouvillons pendant une intervention chirurgicale. 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 1x2 tissue forceps?
The Helmut Zepf 1x2 tissue forceps is a precision surgical instrument designed for oral surgery and guided bone regeneration (GBR) procedures. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, these forceps feature a robust structure adapted to operating room requirements. It is specifically developed to ensure a reliable grip while respecting the integrity of the manipulated structures. This instrument is classified as a Class I medical device, guaranteeing its compliance with regulatory standards for reusable surgical tools. Its stainless steel design ensures optimal durability against the repeated sterilization cycles required in dental practices or hospital environments.
What are the clinical indications for this Helmut Zepf instrument?
This Helmut Zepf tissue forceps is indicated for surgically or atraumatically holding or grasping tissues during complex interventions. Its use is recommended for the precise manipulation of flaps, as well as for holding or removing foreign bodies, sutures, or swabs during the surgical act. In oral surgery and implantology, it allows for rigorous control of soft tissues or suture materials. The instrument is exclusively reserved for qualified healthcare professionals. Its versatility makes it an essential tool for practitioners performing GBR procedures where grip stability is crucial for the success of the intervention and patient safety.
What are the technical characteristics of forceps reference 22.408.20?
The Helmut Zepf tissue forceps, bearing technical reference 22.408.20, is distinguished by its 1x2 configuration which allows for secure fixation without slipping. Manufactured from medical stainless steel, it offers high resistance to corrosion and mechanical stress. Due to its design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, although the user must check for the absence of visible damage before each use. The instrument is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient to guarantee total asepsis during surgical procedures.
What are the contraindications for the use of this stainless steel instrument?
The main contraindication for the use of these forceps lies in patient metal intolerance. Contact with the medical stainless steel instrument may trigger a hypersensitivity reaction or adverse side effects in sensitive subjects. The manufacturer specifies that 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 formally prohibited if it shows visible damage or wear, such as cracks, breaks, or defects on the cutting edges, in order to avoid any traumatic risk to the tissues or tool failure during the procedure.
What are the maintenance and sterilization precautions?
As a non-absorbable and reusable instrument, strict reprocessing precautions apply. All Helmut Zepf instruments must be fully cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to inspect the tool for any signs of wear, corrosion, or deformation before use. The use of damaged products is strictly prohibited. The cleaning process must be meticulous to ensure the elimination of all biological residues. Compatibility with other products used during the intervention must also be verified beforehand by the practitioner. Compliance with these safety instructions is essential to maintain the performance of the medical stainless steel over the long term.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This manufacturer is recognized for its expertise in the production of high-precision surgical instruments. The device complies with medical device regulations and belongs to Class I. As a reusable surgical instrument, it meets the safety and performance requirements defined for this category. The products are delivered non-sterile, leaving the responsibility for final sterilization to the healthcare professional. Traceability is ensured by reference 22.408.20, allowing for precise identification of the model within the Helmut Zepf surgical range distributed by Delynov.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |