Root Elevator Miller - Helmut Zepf (17.100.11) - Delynov

What is the Miller root elevator - Helmut Zepf (17.100.11)?

The Miller root elevator, referenced under code 17.100.11, is a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device, often referred to as a miller syndesmotome in clinical practice, is manufactured from high-quality medical stainless steel. Its structure is specifically designed to meet the requirements of dental and oral surgery. As a Class I instrument, it is part of a range of non-sterile devices requiring a rigorous reprocessing protocol before each use in the dental office or operating theater.

What are the clinical indications for this instrument?

This instrument is indicated for oral surgery procedures requiring the extraction of roots or radicular debris. The miller elevator is particularly useful for the luxation of teeth or fragments remaining after a crown fracture. Its role is to rupture the periodontal ligament fibers and widen the socket through a controlled leverage movement. It is commonly used by dental surgeons and implantologists during avulsion phases, allowing for the preparation of the alveolar site before potential implant placement or bone ridge regularization.

What are the technical characteristics of the 17.100.11 elevator?

The Helmut Zepf Miller root elevator is distinguished by its medical stainless steel construction, a material chosen for its corrosion resistance and its ability to undergo repeated sterilization cycles. The reference code 17.100.11 corresponds to a specific configuration of the working part, adapted for precision maneuvers in posterior or narrow areas. Like all Helmut Zepf products, this instrument is delivered non-sterile. It belongs to the regulatory class Class I, which implies compliance with safety requirements for reusable manual medical devices.

What are the contraindications for the use of this elevator?

The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If a hypersensitivity reaction occurs during the procedure, the process must be immediately interrupted and necessary clinical measures must be taken. It is therefore recommended to check the patient's allergic history before any manipulation.

What are the maintenance and reprocessing precautions?

As a non-resorbable and reusable instrument, particular attention must be paid to the reprocessing cycle. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The practitioner must visually inspect the device for any damage such as cracks, breaks, or wear of the cutting edges. The use of a damaged instrument is strictly prohibited. Due to its robust stainless steel design, there is no defined maximum limit of treatment cycles, as long as the physical integrity of the tool is preserved.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to current regulations. Compliance with cleaning and sterilization protocols is crucial to ensure patient safety and instrument longevity. The use of this Miller root elevator is strictly reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, trained in manual extraction techniques.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.