1. Original product title: RUGINE. INTERCHANGEABLE. - Helmut Zepf (24.751.148) - Delynov 2. Translated product title: RUGINE. INTERCHANGEABLE. - Helmut Zepf (24.751.148) - Delynov

What is the Helmut Zepf interchangeable periosteal elevator?

The Helmut Zepf interchangeable periosteal elevator, referenced under code 24.751.148, is a specific manual instrument intended for oral surgery. Unlike monobloc models, this version is designed to be fixed onto a compatible handle, thus offering flexibility in managing the technical tray. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this elevator instrument is delivered non-sterile. Its structure is optimized to meet the requirements of repeated cleaning and sterilization, characteristic of Class I devices used in a clinical dental environment.

What are the clinical indications for this instrument?

This instrument is primarily indicated as an elevator instrument during invasive surgeries. It is used in the preparation of the surgical site by allowing precise detachment of the mucoperiosteal flap. Its use is common in implantology to expose the alveolar ridge, as well as in periodontal surgery or during complex extractions requiring direct visual access to the bone. As a manual dental instrument, it helps the practitioner separate soft tissues from the bone structure without unnecessarily damaging adjacent tissues, thereby facilitating subsequent drilling or resection steps.

What are the technical characteristics of the 24.751.148 periosteal elevator?

The Helmut Zepf 24.751.148 periosteal elevator is distinguished by its interchangeable design, allowing easy replacement of the working part. It is manufactured from high-quality medical stainless steel, selected for its corrosion resistance and its ability to maintain functional edges after several sterilization cycles. This device belongs to Class I according to medical device regulations. The design allows for complete reprocessing, including cleaning, disinfection, and steam sterilization, in accordance with the rigorous protocols of Helmut Zepf Medizintechnik GmbH to ensure patient safety.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or metal intolerance. As the instrument is composed 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 the necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any use of this elevator instrument in the mouth.

What are the maintenance and reprocessing precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The practitioner must visually inspect the instrument to detect any damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited. Due to the quality of the materials and the design, there is no defined maximum limit of processing cycles, but compatibility with other cleaning products must be verified beforehand.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This device is classified as Class I (Class Ir medical device according to certain reprocessing nomenclatures). It meets strict manufacturing requirements for manual dental instruments in stainless steel. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals. Compliance with cleaning and sterilization protocols is essential to maintain the device's conformity throughout its life cycle in the dental office.

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