Periodontal periosteal elevator - Helmut Zepf (26.182.00)

What is the Helmut Zepf periodontal elevator (26.182.00)?

The Helmut Zepf periodontal elevator, referenced under code 26.182.00, is a high-precision manual dental instrument. Manufactured from medical stainless steel, this dental elevator instrument is designed to withstand repeated cleaning and sterilization cycles. Its structure is specifically adapted to the requirements of oral surgery, offering the practitioner a reliable tool for soft tissue management. As a Class I device, it meets the regulatory requirements for non-invasive or short-term invasive instruments used in dental practices.

What are the clinical indications for this gum detachment instrument?

This instrument is primarily indicated for periodontal and implant surgery procedures. Its major role is to serve as a gum elevator to lift and retract the muco-periosteal flap after the initial incision. It allows for a clean separation between the gum, the periosteum, and the underlying bone surface. The use of this dental elevator instrument is essential for exposing the surgical field during implant placement, treatment of bone defects, or the creation of apically repositioned flaps.

What are the technical characteristics of this Helmut Zepf device?

The 26.182.00 elevator is characterized by its medical-grade stainless steel construction, ensuring optimal biocompatibility during tissue contact. This material allows for complete reprocessing, including cleaning, disinfection, and sterilization. Helmut Zepf Medizintechnik GmbH designed this instrument for ergonomic handling, although the maximum limit of treatment cycles is not defined due to the robustness of the materials used. It belongs to the INSTRU category and is classified as a Class I medical device.

What are the contraindications for the use of this elevator?

The main contraindication related to the use of this Helmut Zepf instrument is known hypersensitivity or intolerance of the patient to metals, specifically medical stainless steel. If a hypersensitivity reaction occurs during the procedure, the manufacturer specifies that the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any use of this manual instrument in contact with gingival or bone tissues.

What maintenance and safety precautions should be observed?

All Helmut Zepf instruments are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. Before each procedure, the practitioner must visually inspect the instrument to detect any potential damage or visible wear, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to ensure patient safety and the effectiveness of the surgical gesture.

Who is the manufacturer and what standards are met?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This elevator is a Class I medical device compliant with current regulations for manual dental instruments. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals. The reprocessing process must follow strict cleaning and sterilization protocols to maintain compliance and safety of use over the long term.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.