Surgical concept Rugine ZEPF - Helmut Zepf (41.888.16) - Delynov

What is the ZEPF design periosteal elevator - Helmut Zepf (41.888.16)?

The ZEPF design periosteal elevator, referenced under code 41.888.16 by Helmut Zepf, is a high-precision manual instrument designed for oral surgery. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this dental elevator is specifically structured to meet the requirements of practitioners during tissue dissection phases. Its robust design allows for controlled manipulation for procedures requiring clean separation of soft tissues from the bone. As a Class I medical device, it meets safety standards for non-invasive or short-term invasive instruments used in dental practices.

What are the clinical indications for this instrument?

This instrument is indicated as a manual dental instrument for various oral, implant, and periodontal surgery procedures. Its primary role is that of a periosteum elevator, allowing for the lifting and retraction of the mucoperiosteal flap after incision. The use of the zepf periosteal elevator is essential for exposing the alveolar ridge during implant placement, bone grafting, or the extraction of impacted teeth. It allows the surgeon visual and instrumental access to the underlying bone structure while minimizing trauma to adjacent soft tissues.

What are the technical characteristics of the 41.888.16 periosteal elevator?

The ZEPF design periosteal elevator (41.888.16) is distinguished by its medical stainless steel construction, a material chosen for its corrosion resistance and its ability to undergo repeated reprocessing cycles. Although specific dimensions are not listed, its ergonomic design by Helmut Zepf ensures optimal grip for periosteal lifting movements. The instrument is delivered non-sterile and must undergo a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient. The durability of the instrument depends on the absence of visible damage such as cracks or defects on the cutting edges.

What are the contraindications for the use of this periosteal elevator?

The main medical contraindication documented by the manufacturer Helmut Medizintechnik GmbH 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 a hypersensitivity reaction is observed during the procedure, the procedure must be stopped immediately and necessary clinical measures must be taken. It is also contraindicated to use the instrument if it shows visible signs of wear, breakage, or damaged cutting edges, as this could compromise patient safety and the effectiveness of the surgical procedure.

What are the maintenance and reprocessing precautions?

As a reusable instrument, rigorous maintenance is mandatory. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit of treatment cycles, as long as the instrument does not show damage or wear. It is imperative to visually inspect the elevator before each procedure to detect any cracks or defects. The use of damaged products is strictly prohibited. This device is exclusively reserved for qualified healthcare professionals mastering asepsis and dental surgery protocols.

Who is the manufacturer and what standards are respected?

The periosteal elevator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with strict regulatory requirements for medical devices. The product is classified as Class I according to current regulations. Compliance with cleaning and sterilization protocols is the responsibility of the healthcare professional to ensure conformity with hospital hygiene standards. Each instrument is engraved with its technical reference (41.888.16) allowing for traceability within the practice. The quality of the medical steel used ensures compatibility with standard autoclave sterilization methods, subject to prior verification of compatibility with other cleaning products.

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