Peeler MOLT FIG.2 Zepf-Line - Helmut Zepf (41.862.12)
Optimize tissue elevation with the MOLT FIG.2 Helmut Zepf
This elevator from the Zepf-Line range offers optimal surgical precision for the manipulation of soft tissues and the periosteum during your oral surgery procedures.
- Model: MOLT FIG. 2 (Ref. 41.862.12).
- Design: 4 mm active tip width for increased efficiency.
- Material: High-quality medical stainless steel for durability and corrosion resistance.
- Ergonomics: Zepf-Line handle designed for a secure grip and precise tactile control.
The Décolleur MOLT FIG.2 Zepf-Line - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.862.12.
- 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 utilisé pour travailler sur la dent / l'appareildentaire lors d'un traitement chirurgical. 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 MOLT FIG.2 Zepf-Line periosteal elevator (41.862.12)?
The MOLT FIG.2 Zepf-Line periosteal elevator, referenced under code 41.862.12 at Delynov, is a high-precision manual dental instrument designed by Helmut Zepf. Also referred to as a raspatorium or raspa in surgical practice, this device belongs to the Zepf-Line range. It is entirely manufactured from medical-grade stainless steel, guaranteeing the robustness required for oral surgery interventions. Its ergonomic design allows for easy handling for demanding practitioners. This Class I medical device is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH, requiring rigorous preparation before any clinical use.
What are the clinical indications for the Helmut Zepf Molt periosteal elevator?
The Molt periosteal elevator (fig. 2) is specifically indicated for dental and oral surgery interventions requiring work on the tooth or dental apparatus. Its primary role as a raspatorium is to allow the precise detachment of soft tissues or the periosteum during surgical treatment. The use of this instrument is exclusively reserved for qualified healthcare professionals. It is used in surgical protocols where a clean and controlled separation of tissues is required. The precision of the 4mm active part (according to the usual technical nomenclature for this model) facilitates access to delicate areas while minimizing tissue trauma.
What are the technical characteristics of this instrument?
This Helmut Zepf periosteal elevator is distinguished by its manufacture from high-quality medical stainless steel. Identified by code 41.862.12, it is part of the Zepf-Line series, recognized for its superior finish. As a manual instrument, it offers optimal tactile feedback during detachment maneuvers. Its monobloc steel structure limits bacterial retention zones, thus facilitating cleaning cycles. It is important to note that this instrument is reusable, although no maximum limit of treatment cycles is defined by the manufacturer due to the intrinsic durability of the materials used and its robust design.
What are the contraindications for the use of this device?
The main contraindication related to the use of this stainless steel periosteal elevator is metal intolerance in the patient. Contact with the instrument may trigger a hypersensitivity reaction. If such a reaction occurs during the surgical procedure, the manufacturer Helmut Zepf specifies that the intervention must be immediately stopped and that the necessary medical measures must be taken accordingly. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage or wear, such as cracks, breaks, or defects on the cutting edges, in order to guarantee patient safety and the effectiveness of the surgical gesture.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use, as well as before each subsequent use. The reprocessing process must be complete and rigorous. Before each use, a visual inspection is essential to detect any signs of degradation or wear. It is crucial to check compatibility with other products used during the intervention. Being delivered non-sterile, strict compliance with the sterilization protocols in force in dental practices is mandatory. Meticulous cleaning before sterilization is the most important step to guarantee the elimination of biological residues.
Who is the manufacturer and what standards are met?
The MOLT FIG.2 periosteal elevator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures traceability and manufacturing quality in accordance with the requirements for manual medical devices for dental surgery. As a Class I product, it meets the essential safety and performance standards for its intended purpose. The use of this instrument is strictly reserved for healthcare professionals, thus guaranteeing an application in accordance with the state of the art in oral surgery and implantology.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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