Root Elevator according to GÄRTNER - Helmut Zepf (17.014.02) - Delynov

What is the Helmut Zepf GÄRTNER root elevator?

The GÄRTNER root elevator, referenced under code 17.014.02, is a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this instrument in the INSTRU category is specifically structured to meet the requirements of extraction surgery. Its robust design allows for precise handling during root luxation phases. As a Class I device, it complies with the rigorous manufacturing standards imposed by European regulations for reusable surgical instruments, thus guaranteeing constant reliability during clinical interventions in dental offices or hospital environments.

What are the clinical indications for this gärtner elevator?

This gärtner elevator is indicated for exodontia procedures requiring the separation of ligament attachments and the mobilization of roots. It is particularly used in oral surgery to facilitate the extraction of fractured or deeply embedded roots. The instrument serves as a lever to widen the socket and break the periodontal ligament, thus preparing the way for forceps. Its application extends to both simple and complex extractions, allowing the surgeon to exert controlled force on the root structure. The use of this Helmut Zepf instrument is strictly reserved for qualified healthcare professionals mastering surgical extraction techniques.

What are the technical characteristics of instrument 17.014.02?

The Helmut Zepf root elevator (reference 17.014.02) is characterized by its medical-grade stainless steel composition, offering optimal resistance to corrosion and mechanical stresses related to luxation. This manual instrument is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. Its ergonomic design is studied to ensure a stable grip, essential for the transmission of force during root elevation. No electronic components or additional accessories are integrated, highlighting its nature as a pure mechanical surgical instrument.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. Contact of the medical stainless steel instrument with an allergic patient can trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary clinical measures must be taken. It is therefore crucial to assess the patient's allergic history before any use. Additionally, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety.

What are the maintenance and reprocessing precautions?

To ensure the safety and longevity of the gartner elevator, a strict reprocessing protocol is required. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before each use. Before treatment, the practitioner must inspect the instrument to detect any wear or visible damage. The use of damaged products is strictly prohibited. Due to the design and materials used for this Class I instrument, there is no defined maximum limit of treatment cycles, as long as the physical integrity of the steel is preserved. Compatibility with other cleaning and sterilization products must also be verified beforehand by the professional user.

Who is the manufacturer and what standards are respected?

The GÄRTNER root elevator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer guarantees that the instrument is designed for professional use and meets quality requirements for manual stainless steel devices. In accordance with the manufacturer's instructions, each product must be rigorously maintained to maintain its compliance with safety standards. Helmut Zepf emphasizes the importance of following the specific instructions for use and safety provided to ensure the performance of the instrument during surgical procedures.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.