Instrument Combine Rugine - Helmut Zepf (24.725.86) - Delynov becomes Rugine Combine Instrument - Helmut Zepf (24.725.86) - Delynov
The Instrument Combine Rugine - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.725.86.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Combined Periosteal Elevator Instrument - Helmut Zepf (24.725.86)?
The combined instrument referenced 24.725.86 is a manual tool designed by Helmut Zepf Medizintechnik GmbH for oral surgery procedures. Manufactured from medical stainless steel, this device belongs to the category of elevation instruments. Its dual structure allows for precise manipulation of soft tissues. As a Class I instrument, it meets the safety requirements for non-invasive or invasive devices for temporary use. This product is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient to ensure the asepsis of the surgical field.
What are the clinical indications for this instrument?
This instrument is indicated for oral, implant, and periodontal surgery procedures requiring access to the bone structure. As a dual dental periosteal elevator, it is primarily used to elevate the mucoperiosteal flap after the incision. It allows the surgeon to cleanly separate the periosteum from the bone without lacerating the surrounding tissues. Its use is common during complex extractions, regularization of alveolar ridges, or preparation of the implant site. The instrument facilitates visibility of the surgical field by keeping soft tissues retracted in a stable manner during the surgical act.
What are the technical characteristics of the Helmut Zepf elevator?
The 24.725.86 model is distinguished by its combined configuration, offering two functional ends to optimize the workflow. Manufactured by Helmut Zepf Medizintechnik GmbH, it uses medical stainless steel selected for its corrosion resistance and its ability to withstand repeated sterilization cycles. Its ergonomic design aims to provide a secure grip for delicate elevation movements. Although there is no defined maximum limit for processing cycles due to the robustness of the materials, the instrument must be inspected before each use to detect any cracks, breaks, or defects on the active parts.
What are the contraindications for the use of this instrument?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals, specifically to medical stainless steel. If an allergic reaction or hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be stopped immediately. Necessary clinical measures must then be taken accordingly. It is therefore recommended to check the patient's allergic history before any surgical intervention involving this manual instrument.
What are the maintenance and reprocessing precautions?
As the instrument is delivered non-sterile, a strict reprocessing protocol is mandatory. Before the first use and after each intervention, the elevator must be cleaned, disinfected, and sterilized. The practitioner must check compatibility with other cleaning products used. A visual inspection is crucial: any instrument showing visible damage, such as cracks or excessive wear of the edges, must never be used. The lifespan of the instrument depends on compliance with these maintenance instructions and handling in accordance with its intended use in a dental office or hospital environment.
Who is the manufacturer and what standards are met?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. The product is classified as a Class I medical device according to current regulations. It is designed to be used exclusively by qualified healthcare professionals in dental surgery. The manufacturer emphasizes the importance of following safety and use instructions to maintain the integrity of the device. Traceability is ensured by the technical reference 24.725.86, guaranteeing the origin and compliance of the equipment with Helmut Zepf manufacturing standards.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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