Narrow 13 cm Dissection Forceps - Helmut Zepf (22.230.13) - Delynov
Product features
The Pinces à dissection étroite de 13 cm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.230.13.
- 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 narrow dissecting forceps?
The Helmut Zepf narrow dissecting forceps, referenced under code 22.230.13, is a high-precision manual dental instrument designed for oral surgery procedures. Manufactured from premium quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, these forceps are distinguished by their narrow structure adapted for delicate manipulations. This medical device belongs to Class I and is specifically developed to meet the requirements of healthcare professionals during Guided Bone Regeneration (GBR) procedures. Its robust design ensures reliable handling of soft tissues during dissection phases.
What are the clinical indications for this instrument?
This instrument is indicated as a manual dental instrument for surgical procedures requiring precise tissue dissection. Its use is particularly relevant in the context of implant surgery and periodontology, notably for GBR protocols. It allows the practitioner to manipulate anatomical structures with great finesse. The use of this device is strictly reserved for qualified healthcare professionals. It is imperative to check the integrity of the instrument, such as the absence of cracks or defects on the edges, before each intervention to guarantee patient safety.
What are the technical characteristics of the 22.230.13 forceps?
The Helmut Zepf narrow dissecting forceps has a total length of 13 cm, offering an optimal balance between ergonomics and control during the surgical act. It is entirely designed in medical stainless steel, a material chosen for its durability and resistance to processing cycles. This specific model (reference 22.230.13) has a narrow tip facilitating access to restricted areas of the oral cavity. Due to its design and the materials used, the manufacturer does not establish a defined maximum limit for the number of achievable processing cycles, provided that the instrument shows no visible wear.
What are the contraindications for the use of this device?
The main contraindication for the use of these forceps lies in patient metal intolerance. Contact with medical stainless steel can trigger a hypersensitivity reaction or undesirable side effects. If such a reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, it is formally prohibited to use the instrument if it shows visible damage, such as breaks or deformations, as this could compromise clinical safety and dissection efficiency.
What are the maintenance and sterilization precautions?
Helmut Zepf products are delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. It is crucial to carefully clean each product to remove any residue before the sterilization process. The practitioner must inspect the instrument to detect possible damage or signs of wear, such as defects on the cutting edges. Compatibility with other products used during the intervention must also be verified beforehand to ensure effective and secure reprocessing.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer guarantees that the instrument is designed for professional use in a dental environment, respecting strict manufacturing protocols for medical stainless steel. As a Class I instrument, it meets the safety and performance requirements defined for manual dental instruments. Each forceps is identified by a unique technical reference (22.230.13) allowing precise traceability within the dental practice.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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