RUGINE. INTERCHANGEABLE. - Helmut Zepf (24.751.147) - Delynov Website Dental Surgery Products

What is the Helmut Zepf interchangeable periosteal elevator?

The Helmut Zepf interchangeable periosteal elevator, referenced under code 24.751.147, is a precision manual instrument used in oral surgery. It consists of an active part designed to be mounted on a compatible handle, thus offering flexibility of use and facilitated maintenance. Manufactured by Helmut Zepf Medizintechnik GmbH in medical stainless steel, it guarantees the necessary resistance to mechanical stress during the detachment of soft tissues from the alveolar bone. This device belongs to the category of interchangeable consumables for the dental operating block.

What are the clinical indications for this instrument?

This instrument is indicated for all procedures requiring the elevation of a mucoperiosteal flap. In implantology, it allows for clean clearance of the surgical site for bone exposure before drilling. In periodontal or oral surgery, it is used to detach the periosteum without lacerating the tissues, thus facilitating access during complex extractions or apical resection surgeries. Its interchangeable nature allows the practitioner to adapt the tip according to the anatomy of the site or the surgical technique employed.

What are the technical characteristics of the 24.751.147 periosteal elevator?

The Helmut Zepf 24.751.147 periosteal elevator is distinguished by its modular design. It is manufactured from medical grade stainless steel, a material chosen for its mechanical properties and its compatibility with sterilization cycles. As a manual instrument, it does not include a needle. Its structure is designed to provide a stable support point during levering or scraping movements. Like all products from the manufacturer, it is delivered non-sterile and requires a complete cleaning and sterilization protocol before its first use in the practice.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, specifically medical stainless steel. If a hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be immediately stopped and the necessary clinical measures must be taken. It is also contraindicated to use the instrument if it shows visible damage such as cracks, breaks, or defects on the edges, as this could compromise patient safety.

What are the maintenance and reprocessing precautions?

Being a non-resorbable and reusable instrument, the periosteal elevator must undergo a complete cycle of cleaning, disinfection, and sterilization before each use. The manufacturer specifies that there is no defined maximum limit of treatment cycles, as this depends on actual wear and visible damage. Before each intervention, the practitioner must inspect the instrument to detect any trace of corrosion or deformation. The use of damaged products is strictly prohibited. Compatibility with other products of the interchangeable system must also be verified beforehand to ensure the safety of the assembly.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device (Class Ir according to the mentioned nomenclature). In accordance with regulatory requirements, the instrument is intended exclusively for professional use by qualified healthcare practitioners. The manufacturer insists on strict compliance with the safety and usage instructions provided, particularly regarding the reprocessing of devices delivered non-sterile, in order to guarantee compliance with hospital and dental hygiene standards.

State of the art

Surgical medical consumables play a decisive role in operative safety.