Dissection Forceps Helmut Zepf (22.200.13) - Delynov
The Pinces à dissection Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.200.13.
- 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 Helmut Zepf (22.200.13) dissection forceps?
The Helmut Zepf dissection forceps, referenced under code 22.200.13, is a high-precision manual dental instrument designed for oral surgery interventions, particularly in Guided Bone Regeneration (GBR) procedures. Manufactured from premium quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument is specifically developed to meet the requirements of healthcare professionals. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient. Its robust stainless steel design ensures optimal longevity, although no maximum limit for reprocessing cycles is defined by the manufacturer due to the nature of the materials used.
What are the clinical indications for this instrument?
This instrument is indicated as a manual dental instrument for oral surgery procedures. Its use is primarily intended for the delicate manipulation of tissues during dissection phases or during implant surgery and bone reconstruction (GBR) protocols. As a Class I medical device, it is exclusively reserved for use by qualified healthcare professionals. The practitioner must ensure the compatibility of the forceps with other products used during the intervention. It is imperative to check the condition of the instrument before each procedure: the presence of visible damage, cracks, breaks, or defects on the cutting edges must lead to the immediate removal of the product to guarantee operative safety.
What are the technical characteristics of the 22.200.13 forceps?
The Helmut Zepf dissection forceps (22.200.13) is distinguished by its medical stainless steel construction, a reference material for dental surgical instrumentation. This choice of material guarantees the mechanical resistance necessary for precise intraoral manipulations. Categorized as Class I according to regulatory directives, this manual instrument does not have needle specifications as it is not a suture. Its structure is designed to offer an ergonomic grip for the surgeon. The manufacturer, Helmut Zepf Medizintechnik GmbH, emphasizes that the lifespan of the instrument depends on maintenance and the absence of visible wear. Any product showing signs of technical degradation must be replaced to maintain standards of care.
What are the contraindications for the use of this device?
The main contraindication related to the use of this Helmut Zepf dissection forceps is patient metal intolerance. Contact with medical stainless steel can, in certain cases, trigger a hypersensitivity reaction or an allergic reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken accordingly. Furthermore, the use of the instrument is strictly prohibited if it shows visible damage such as cracks or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the surgical gesture. Use is limited to trained healthcare professionals.
What are the maintenance and reprocessing precautions?
As this is a non-absorbable and reusable instrument, strict reprocessing precautions apply. Helmut Zepf products are delivered non-sterile. It is mandatory to perform complete cleaning, disinfection, and sterilization before the first use and after each subsequent use. The manufacturer specifies that due to the design and materials, it is not possible to define a maximum limit of achievable reprocessing cycles. However, practitioner vigilance is required: each product must be inspected before use to detect any signs of wear or corrosion. The use of damaged or worn products is formally prohibited to avoid any risk of complication during dental care.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is listed under Class I (Class Ir according to certain reprocessing nomenclatures). It meets the regulatory requirements for manual dental instruments. The manufacturer imposes strict safety instructions, notably the obligation of prior sterilization and compliance with professional use indications. The traceability and quality of the medical stainless steel used comply with the standards expected for precision surgical instrumentation. By choosing reference 22.200.13 from Delynov, practitioners ensure they have a tool that complies with Helmut Zepf brand directives.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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