Rugine Linguale Dental Instrument Combine - Helmut Zepf (24.747.07OX)

What is the Helmut Zepf 24.747.07OX lingual periosteal elevator?

The Helmut Zepf lingual periosteal elevator, referenced under code 24.747.07OX, is a high-precision manual dental instrument belonging to the category of reusable consumables. This device is manufactured from medical stainless steel, a standard material for surgical instrumentation ensuring the robustness required for oral surgery procedures. As a dental elevator, this instrument is specifically designed for practitioners requiring a reliable tool for flap management. It is part of the Class I range of devices developed by Helmut Zepf Medizintechnik GmbH to meet the technical needs of dental practices and hospital centers.

What are the clinical indications for this instrument?

This instrument is indicated for use as a manual dental instrument during various oral surgery procedures. Its primary role is to serve as a dental elevator to gently separate the periosteum from the alveolar bone, particularly in difficult-to-access areas such as the lingual aspect. It is used during the preparation of implant sites, periodontal surgeries, or complex extractions requiring flap reflection. The lingual periosteal elevator allows for clean and controlled detachment, limiting unnecessary tissue trauma while providing the surgeon with a grip adapted to the anatomical constraints of the oral cavity.

What are the technical characteristics of the 24.747.07OX periosteal elevator?

The Helmut Zepf lingual periosteal elevator is distinguished by its medical stainless steel construction, ensuring optimal resistance to corrosion and repeated sterilization cycles. This combined model is identified by technical reference 24.747.07OX. Although the manufacturer does not define a maximum limit for processing cycles due to the design and materials used, the instrument must be inspected before each use. The practitioner must check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to guarantee surgical safety.

What are the contraindications for the use of this device?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient may 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 clinical measures must be taken. It is therefore imperative to check the patient's allergic history before any use. Apart from this material-related contraindication, use is reserved exclusively for qualified healthcare professionals.

What are the maintenance and sterilization precautions?

Helmut Zepf instruments are delivered non-sterile and require a strict protocol before any use. They must 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 any residue before the sterilization cycle. It is also necessary to verify compatibility with other products used simultaneously. Due to its metallic nature, reprocessing must follow current standards for Class I instrumentation to maintain the integrity of the stainless steel and ensure the essential asepsis in a surgical environment.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. The product is classified as a Class I medical device according to current regulations. The manufacturer complies with safety and performance requirements for manual dental instruments. Each periosteal elevator is subjected to rigorous quality controls to ensure it meets clinical standards. As a Class I device, it is designed for professional use by trained practitioners, guaranteeing traceability and compliance with European Union manufacturing requirements for reusable surgical instruments.

State of the art

Surgical medical consumables play a decisive role in operative safety.