University of Minnesota Retractor - Helmut Zepf (37.437.15)
Product features
The Écarteur Université de Minnesota - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 37.437.15.
- 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 Un instrument pour maintenir la zone chirurgicale ouverte. 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 University of Minnesota retractor?
The University of Minnesota retractor, referenced under code 37.437.15, is a precision surgical instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from high-quality medical stainless steel, this device is specifically structured to offer optimal robustness and durability during interventions. As a manual instrument, it features ergonomics adapted to the requirements of oral surgery. This equipment belongs to the category of instruments (INSTRU) and benefits from the expertise of the Helmut Zepf brand in the field of medical instrumentation. Its stainless steel composition ensures the necessary resistance to repeated cleaning and sterilization cycles, while guaranteeing safe handling for the practitioner.
What are the clinical indications for this instrument?
According to data from the manufacturer Helmut Zepf Medizintechnik GmbH, the intended purpose and primary indication of this instrument are to keep the surgical area open. In oral, implant, or dental surgery, the University of Minnesota retractor allows for the retraction of soft tissues, such as cheeks or mucoperiosteal flaps, in order to provide the surgeon with maximum visibility and clear access to the operative site. Its use is strictly reserved for qualified healthcare professionals. It is essential for securing the operative field and facilitating technical maneuvers during invasive procedures. The instrument must be systematically checked before use to detect any visible damage, such as cracks or defects on the edges, to ensure patient safety.
What are the technical characteristics of the 37.437.15 retractor?
The University of Minnesota retractor (reference 37.437.15) is characterized by its medical stainless steel construction, a material chosen for its mechanical properties and compatibility with hospital disinfection protocols. This device is classified as a Class I instrument according to current regulations. It is delivered non-sterile by the manufacturer Helmut Zepf and requires complete processing before its first use, as well as after each intervention. 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 inspect the instrument to identify any premature wear or breakage that would make the product unusable.
What are the contraindications for the use of this retractor?
The main contraindication mentioned by the manufacturer concerns hypersensitivity to metals. An intolerance in the patient may result from direct contact with the medical stainless steel instrument, potentially triggering a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken accordingly. Furthermore, it is formally forbidden to use the instrument if it presents visible damage, cracks, breakages, or defects on the cutting edges. The use of damaged or worn products compromises clinical safety and the integrity of the tissues manipulated during surgery.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, and then after each subsequent use. The reprocessing process must be complete and rigorous: thorough cleaning is crucial before sterilization to guarantee the elimination of any residue. Before each use, the healthcare professional must verify compatibility with other products used simultaneously. As the retractor is delivered non-sterile, strict compliance with hygiene protocols is a sine qua non condition for its use in the operating room. The durability of the instrument depends directly on the quality of cleaning and the absence of mechanical damage noted during the mandatory visual inspection.
Who is the manufacturer and what standards are respected?
The University of Minnesota retractor is produced by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device complies with Class I of the medical device regulations. The manufacturer emphasizes that its products are intended exclusively for healthcare professionals. Each instrument is designed to meet the safety and performance requirements expected in the most demanding surgical environments. Although the specific CE marking is not detailed in the sources provided, compliance with Class I and adherence to the manufacturer's maintenance instructions guarantee a high level of reliability for dental surgeons and implantologists using the Helmut Zepf catalog.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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