Micro Preccelle D'APRES COOLEY - Helmut Zepf (22.815.17) - Delynov (Dental Surgery Products)
Product features
The Micro Precelle D'APRES COOLEY - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.815.17.
- 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 Micro Precelle D'APRES COOLEY Helmut Zepf?
The Micro Precelle D'APRES COOLEY, referenced under code 22.815.17 by Helmut Zepf, is a precision surgical instrument designed for delicate interventions. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this forceps is distinguished by its robust structure and meticulous finish. It belongs to the category of Class I surgical consumables. This device is specifically developed to offer reliable handling during critical phases of surgery, guaranteeing a stable grip while respecting the integrity of the manipulated structures. Its stainless steel design ensures longevity and resistance to repeated cleaning cycles, thus meeting the rigorous requirements of technical platforms in oral and implant surgery.
What are the clinical indications for this instrument?
The intended use for the Micro Precelle D'APRES COOLEY Helmut Zepf is strictly defined as a surgical instrument allowing for the atraumatic or surgical holding or grasping of soft tissues. It is also indicated for the handling, holding, or removal of foreign bodies, sutures, or swabs during surgical procedures. In oral surgery, its role is crucial for stabilizing flaps or assisting the practitioner during the placement of suture devices. The Cooley design allows for a precise approach, limiting unnecessary tissue trauma. This device is exclusively reserved for use by qualified healthcare professionals trained in specific surgical protocols.
What are the technical characteristics of reference 22.815.17?
Technical reference 22.815.17 corresponds to a micro forceps based on the Cooley design, produced by Helmut Zepf. Its main characteristic lies in its manufacture from medical stainless steel, a material chosen for its mechanical properties and its compatibility with sterilization processes. The instrument is delivered non-sterile and requires complete processing before its first use. Due to its specific design and the materials used, the manufacturer specifies that there is no defined maximum limit for the number of achievable processing cycles, although the user must systematically check for the absence of visible damage, such as cracks, breaks, or defects on the edges before each intervention.
What are the contraindications for the use of this forceps?
The main contraindication related to the use of this medical stainless steel instrument concerns metal intolerance in the patient. Contact with the instrument can trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, 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 or wear, notably cracks or structural defects. It is imperative never to use damaged products to guarantee patient safety and the effectiveness of the surgical act.
What maintenance and safety precautions must be followed?
To guarantee the safety and performance of the Micro Precelle Helmut Zepf, all instruments must imperatively be cleaned, disinfected, and sterilized before their first use as well as before each subsequent use. The manufacturer emphasizes the vital importance of complete cleaning to eliminate all residue. Before each use, a meticulous visual inspection is required to detect possible signs of wear, such as cracks or breaks on the jaws or the body of the forceps. Compatibility with other products used simultaneously during surgery must also be verified beforehand. Compliance with these safety instructions is essential to maintain the integrity of Class I instrumentation.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to current regulations. As a renowned manufacturer, Helmut Zepf applies rigorous manufacturing protocols to ensure the compliance of its surgical instruments. The products are delivered non-sterile, leaving the responsibility for final reprocessing to the healthcare professional. Compliance with the instructions provided by the manufacturer regarding cleaning, disinfection, and sterilization is mandatory to guarantee that the instrument retains its functional properties and meets the clinical safety requirements expected for devices in this category.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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