Peeler MOLT FIG.2 Zepf-Line - Helmut Zepf (41.862.12)
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.
What is the MOLT FIG.2 Zepf-Line elevator?
The MOLT FIG.2 Zepf-Line elevator, referenced under code 41.862.12, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this device belongs to the Zepf-Line range, recognized for its manufacturing quality. Its structure consists of an ergonomic handle and a specific Molt-type working part, also called a raspatorium or raspa in the surgical field. This instrument is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient to ensure aseptic safety during oral surgery procedures.
What are the clinical indications?
This instrument is indicated for all oral surgery procedures requiring precise management of soft tissues and the periosteum. The molt elevator is primarily used to detach the mucoperiosteal flap from the bone surface, thereby facilitating visual and instrumental access to the surgical site. It is employed during complex extractions, guided bone regeneration surgeries, or implant placements. Its function as a raspatorium allows for a clean separation of tissues without excessive lacerations, which is crucial for post-operative healing. Its use is strictly reserved for healthcare professionals qualified in dentistry and maxillofacial surgery.
What are the technical specifications?
The MOLT FIG.2 elevator (reference 41.862.12) is distinguished by a 4mm working end, often referred to as a grosser raspa in technical nomenclatures. This 4mm width allows for stable support on the bone during periosteum elevation. Manufactured by Helmut Zepf, the instrument uses medical stainless steel selected for its corrosion resistance and durability against repeated sterilization cycles. The Zepf-Line design integrates meticulous finishes on the cutting edges to maintain constant efficiency. As a manual instrument, it does not contain electronic components or complex mechanisms, relying on the reliability of its monobloc design.
What are the contraindications for use?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the tissues of an allergic patient may trigger a hypersensitivity reaction. If such a reaction occurs during the surgical act, the procedure must be immediately interrupted and appropriate medical measures must be taken. Furthermore, the use of the instrument is prohibited if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the procedure.
What are the maintenance and reprocessing precautions?
As Helmut Zepf products are delivered non-sterile, they must imperatively undergo a full reprocessing cycle before the first use. This includes cleaning, disinfection, and steam sterilization. It is imperative to visually inspect the dental periosteal elevator before each use to detect any signs of wear or corrosion. Due to its robust stainless steel design, there is no defined maximum limit of treatment cycles, but the lifespan depends directly on compliance with maintenance protocols. Any blunt or damaged instrument must be removed from service to avoid any clinical risk.
Who is the manufacturer and what standards are met?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. The MOLT FIG.2 elevator is classified as a Class I medical device according to current regulations. It meets the manufacturing requirements for manual dental instruments intended for surgery. Compliance with cleaning and sterilization protocols is the responsibility of the practitioner, in accordance with the instructions provided by Helmut Zepf. This Class I status confirms that the product meets the basic safety and performance standards for non-invasive or temporary invasive instruments in the dental office.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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