The Decoller Molt Figure 1 Zepf-Line - Helmut Zepf (41.862.11) - Delynov
The Décolleur Molt Figure 1 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: 41.862.11.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Molt Figure 1 periosteal elevator?
The Molt Figure 1 periosteal elevator, referenced under code 41.862.11, is a manual instrument from the Zepf-Line range manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this device is specifically developed to meet the requirements of oral surgery. Its structure allows for rigorous manipulation of soft tissues. As an instrument in the INSTRU category, it is distinguished by a design adapted to specialized clinical environments. This Figure 1 model is part of the technical arsenal used by dental surgeons for the initial phases of surgical site exposure, ensuring effective flap management.
What are the clinical indications?
This instrument is indicated for all oral, periodontal, or implant surgery procedures requiring the elevation of a full-thickness flap. Its primary use lies in the detachment of the periosteum from the alveolar bone. It is used during complex extractions, implant placement, or in the context of pre-implant surgeries. The Molt Figure 1 periosteal elevator allows the practitioner to separate soft tissues systematically, thus providing optimal visibility of the bone ridge. Its application is strictly reserved for qualified healthcare professionals mastering oral surgery protocols.
What are the technical characteristics?
The Molt Figure 1 periosteal elevator (reference 41.862.11) is manufactured from high-quality medical stainless steel by Helmut Zepf. This material ensures the robustness necessary for the leverage forces applied during mucoperiosteal detachment. The instrument is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. The Zepf-Line design emphasizes device durability, although no maximum limit of processing cycles is defined. It is crucial to inspect the instrument before each use to detect any cracks, breaks, or defects on the edges.
What are the contraindications for use?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is made of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and appropriate medical measures must be taken. Additionally, the use of the instrument is contraindicated if it presents visible damage such as cracks or excessive wear of the active parts, in order to guarantee patient safety and the effectiveness of the surgical gesture.
What are the maintenance and reprocessing precautions?
Being a non-resorbable and reusable instrument, the Molt Figure 1 periosteal elevator requires a strict reprocessing protocol. Before any use, it must be cleaned, disinfected, and sterilized according to current standards. The manufacturer specifies that due to the product design and materials used, it is not possible to define a maximum limit of sterilization cycles. However, the longevity of the device depends on the absence of visible damage. It is imperative to check compatibility with other cleaning and sterilization products beforehand. Any damaged or worn instrument must be immediately removed from service to avoid any clinical risk.
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 Molt Figure 1 periosteal elevator is classified as a Class I medical device (Class Ir according to the nomenclature mentioned). It meets the regulatory requirements relating to manual dental instruments. Compliance with the safety and use instructions provided by Helmut Zepf is essential to guarantee the conformity of the device during its professional use. As a Class I product, it follows the rigorous manufacturing and quality control protocols imposed for reusable surgical instruments in Europe.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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