Root Elevator according to GÄRTNER - Helmut Zepf (17.013.01) - Delynov

What is the GÄRTNER root elevator - Helmut Zepf?

The GÄRTNER root elevator, referenced under code 17.013.01, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is specifically developed to meet the requirements of oral surgery during extraction phases. Its robust structure allows for rigorous handling for practitioners seeking a reliable device. As a Helmut Zepf brand instrument, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation. This model is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before each use to ensure safety within the practice.

What are the clinical indications for this instrument?

This dental gartner elevator is primarily indicated for dental extraction procedures, particularly for the luxation of roots and root fragments. In oral and implant surgery, it is used to separate the root from its alveolar attachment by applying moderate leverage force. Its use is reserved for qualified healthcare professionals. The instrument allows for addressing various clinical cases where simple extraction with forceps is insufficient, thus facilitating the clearing of dental structures before potential implant placement or to sanitize an infected site. The integrity of the instrument, including the absence of cracks or defects on the edges, should be checked before any clinical intervention.

What are the technical characteristics of the 17.013.01 elevator?

The Gärtner root elevator (reference 17.013.01) is distinguished by its high-quality medical stainless steel construction. It belongs to Class I of medical devices according to current regulations. Although specific dimensions are not detailed, its design is optimized for manual grip and efficient force transmission during luxation. This Helmut Zepf product is designed to withstand repeated reprocessing cycles, including cleaning and sterilization, without a maximum number of cycles defined by the manufacturer, subject to prior visual inspection. The absence of visible damage such as breaks or excessive wear is imperative to maintain its technical performance.

What are the contraindications for using this elevator?

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 necessary medical measures taken. Apart from this specific sensitivity to metallic components, use is prohibited if the instrument shows signs of wear, cracks, or defective cutting edges, as this could compromise patient safety and the effectiveness of the surgical procedure.

What are the maintenance and sterilization precautions?

Like any non-sterile Class I instrument, this Helmut Zepf root elevator requires a strict protocol. Before the first use and after each subsequent use, it must be cleaned, disinfected, and sterilized. The manufacturer emphasizes the importance of cleaning each product before proceeding to sterilization to remove all organic residue. It is crucial to check for the absence of visible damage, such as cracks or defects on the active parts, before each cycle. The use of damaged or worn products is strictly prohibited. Compatibility with other cleaning and sterilization products must also be verified beforehand by the healthcare professional responsible for reprocessing.

Who is the manufacturer and what standards are respected?

The GÄRTNER root elevator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with requirements for manual stainless steel dental instruments. As a Helmut Zepf product, it follows rigorous manufacturing processes compliant with European standards for medical devices. Professionals can refer to the manufacturer's instructions regarding the intended purpose and safety guidelines to ensure usage compliant with health regulations. Maintaining compliance relies on an appropriate reprocessing cycle and constant monitoring of the instrument's physical condition by the end user.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.