Anatomical Tweezers Helmut Zepf for (22.200.14) - Delynov
The Pince anatomique Helmut Zepf pour is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.200.14.
- 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 anatomical forceps (22.200.14)?
The Helmut Zepf anatomical forceps, referenced under code 22.200.14 at Delynov, is a high-precision manual dental instrument designed for oral surgery and guided bone regeneration (GBR) procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, these forceps are made of high-quality medical stainless steel to ensure durability and optimal tissue handling. This medical device belongs to Class I. It is specifically developed to meet the requirements of healthcare professionals seeking a reliable instrument for gripping and holding soft tissues or filling materials during complex surgical protocols.
What are the clinical indications for this instrument?
These anatomical forceps are indicated as a manual dental instrument for various oral surgery procedures. Its primary use concerns the delicate manipulation of tissues during dissection or suturing phases, as well as the placement of devices within the framework of guided bone regeneration (GBR). As a precision instrument, it allows the dental surgeon or implantologist to operate with great dexterity. The manufacturer Helmut Zepf specifies that this device is exclusively reserved for qualified healthcare professionals, thus guaranteeing use in accordance with current clinical standards in implantology and periodontology.
What are the technical characteristics of the 22.200.14 forceps?
The Helmut Zepf 22.200.14 anatomical forceps are distinguished by their medical stainless steel composition, a material chosen for its resistance and compatibility with repeated sterilization processes. Although the manufacturer does not define a maximum limit for processing cycles due to the robustness of the materials used, the instrument must undergo rigorous inspection before each use. It is imperative to check for the absence of visible damage such as cracks, breaks, or defects on the active parts. Any instrument showing signs of wear or structural damage must never be used in order to guarantee patient safety and the effectiveness of the surgical procedure.
What are the contraindications for the use of this device?
The main contraindication related to the use of this medical stainless steel instrument is metal intolerance in the patient. Contact with the instrument may trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. Furthermore, the use of the forceps is contraindicated if the instrument presents visible defects, cracks, or damaged cutting edges. Strict compliance with these safety instructions is essential to prevent any undesirable side effects during dental care.
What are the maintenance and sterilization precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. Before the first use and for each subsequent use, the instrument must undergo a complete cycle of cleaning, disinfection, and sterilization. It is crucial to clean each product before it goes into the autoclave. The manufacturer emphasizes that reprocessing depends on the product design and materials; however, the user must check compatibility with other products used simultaneously. Rigorous maintenance ensures the longevity of the stainless steel and maintains the gripping performance necessary for oral surgery interventions.
Who is the manufacturer and what standards are respected?
These forceps are manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (or Class Ir according to the mentioned technical marking MDC0483). The manufacturer complies with strict regulatory requirements for manual dental instruments, guaranteeing traceability and manufacturing quality. As a Class I device, it meets the safety and performance standards for professional use in dental practices or hospital environments. Each instrument is designed to offer optimal ergonomics while respecting the rigorous hygiene protocols imposed by European medical device regulations.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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