Figure 24G Glickmann Type Surgical Scaler - Helmut Zepf (41.862.21)
The Décolleur Glickmann Figure 24G - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.862.21.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the Glickmann Figure 24G periosteal elevator?
The Glickmann Figure 24G periosteal elevator is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed for oral surgery, this instrument is made of medical-grade stainless steel, ensuring resistance adapted to the stresses of clinical interventions. It consists of an ergonomic handle and specific working ends allowing for the manipulation of soft tissues. As a Class I medical device, it meets the quality requirements for reusable instruments. This model, referenced under code 41.862.21, is a standard tool for practitioners performing flap surgeries or complex extractions requiring a clean separation of the periosteum.
What are the clinical indications?
This glickmann elevator is indicated for any surgical intervention requiring work on the tooth or dental apparatus. Its primary use lies in the elevation and retraction of the mucoperiosteal flap to expose the alveolar bone. It is particularly used during implant surgeries, surgical periodontology, or dental extractions requiring direct visual access. The instrument allows for the delicate separation of the gingiva from the bone surface without unnecessarily lacerating the tissues. Its use is strictly reserved for qualified healthcare professionals mastering oral and maxillofacial surgery techniques.
What are the technical characteristics of this instrument?
The Glickmann Figure 24G periosteal elevator (reference 41.862.21) is characterized by its manufacture from high-quality medical stainless steel, selected by Helmut Zepf for its durability and compatibility with sterilization processes. It is a non-sterile manual instrument upon delivery, requiring a full preparation cycle before each use. The design of the instrument does not define a maximum limit of processing cycles, as this depends on visible wear and maintenance. Practitioners must inspect the instrument before each use to detect potential damage such as cracks, breaks, or defects on the cutting edges.
What are the contraindications for use?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or metal intolerance in the patient. Since the instrument is composed of medical stainless steel, contact may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any surgical manipulation with this instrument.
What are the maintenance and sterilization precautions?
Like any reusable surgical instrument, the Glickmann elevator must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The manufacturer emphasizes the importance of thorough cleaning to remove all biological residues. Before each use, it is crucial to check for the absence of visible damage, cracks, or premature wear. The use of damaged or worn products is strictly prohibited. Due to the materials used, there is no fixed limit for sterilization cycles, but the lifespan of the instrument depends on its handling and compliance with standardized decontamination protocols in a medical environment.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This elevator is classified as a Class I medical device according to current regulations. Helmut Zepf products are delivered non-sterile and must undergo rigorous reprocessing by the healthcare professional. Compliance with safety standards relies on strict maintenance and use in accordance with the intended purpose, namely manual instrumentation during dental surgical treatments. Traceability is ensured by the technical reference 41.862.21.
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