Product Title: INTERCHANGEABLE RUGINE - Helmut Zepf (24.751.149)

What is the Helmut Zepf INTERCHANGEABLE PERIOSTEAL ELEVATOR?

The Helmut Zepf interchangeable periosteal elevator, referenced under code 24.751.149, is a manual instrument designed for oral surgery. This device consists of a removable active part, allowing for flexibility of use during clinical procedures. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument is delivered non-sterile and requires a complete cycle of cleaning, disinfection, and sterilization before any use. Its interchangeable design facilitates instrumentation maintenance by allowing the specific replacement of the working end without changing the entire handle, thus ensuring efficient management of the dental practice's instrument pool.

What are the clinical indications for this dental elevator?

This dental elevator is indicated for procedures requiring the elevation of a full-thickness flap. In implant or periodontal surgery, the dental surgery periosteal elevator is used to detach the periosteum from the cortical bone after the initial incision. It thus allows the surgical field to be exposed for implant placement, bone grafting, or the treatment of periodontal defects. The use of this instrument is strictly reserved for qualified healthcare professionals who have mastered soft and hard tissue manipulation techniques in the oral environment. Its role is decisive in ensuring optimal visibility and secure access to anatomical structures during tissue detachment phases.

What are the technical characteristics of reference 24.751.149?

Technical reference 24.751.149 corresponds to a specific periosteal elevator from the Helmut Zepf range. It is distinguished by its interchangeable mechanism that fits the manufacturer's compatible handles. The instrument is made of high-quality medical stainless steel, selected for its resistance to repeated sterilization cycles. As a Class I device, it meets regulatory safety requirements for non-invasive or invasive manual instruments for temporary use. The manufacturer does not define a maximum limit for processing cycles but emphasizes the importance of a rigorous visual inspection before each use to detect any cracks, breaks, or wear of the cutting edges that could compromise the effectiveness of the surgical maneuver.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns patients with a known intolerance or hypersensitivity to metals, particularly medical stainless steel. Contact of the instrument with tissues can trigger an allergic reaction in these subjects. If such a hypersensitivity reaction occurs during the procedure, the procedure must be immediately interrupted and the necessary medical measures must be taken accordingly. It is therefore recommended to evaluate the patient's allergic history during the preoperative anamnesis. Furthermore, the use of an instrument showing visible damage (cracks, surface defects) is strictly prohibited to avoid any risk of complication.

What are the maintenance and sterilization precautions?

Like any reusable dental surgery instrument, this periosteal elevator must follow a strict reprocessing protocol. Products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, and then after each subsequent use. Cleaning must be complete to eliminate any biological residue before autoclaving. It is crucial to check compatibility with other cleaning and disinfection products used. The manufacturer insists on checking the condition of the instrument: any sign of premature wear or degradation of the sharp edges must lead to the disposal of the interchangeable part in order to guarantee patient safety and the precision of the surgical act.

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 product is classified as a Class I medical device according to current regulations. Compliance with manufacturing standards ensures that the instrument meets the safety and performance requirements for its intended purpose as a manual dental instrument. Traceability is ensured by reference 24.751.149. As a Class I device, it is designed to be used exclusively by trained healthcare professionals. The manufacturer emphasizes that the service life of the instrument depends on the frequency of use and compliance with the cleaning and sterilization instructions recommended in the technical manual.

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Surgical medical consumables play a decisive role in operative safety.