Elevator X - Luxa - Tool - Curved - 7 - Helmut Zepf (17.007.07) - Delynov

What is the X - Luxa Elevator - Instrument - Curved - 7 - Helmut Zepf (17.007.07)?

The X - Luxa Elevator, referenced under code 17.007.07, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool comes in a curved luxator form specifically studied for extraction procedures. Its robust structure and meticulous finish meet the requirements of oral surgery professionals. As a Class I device, it is intended for strict professional use in dental offices or hospital settings for luxation and elevation procedures.

What are the clinical indications for this instrument?

The use of this luxating elevator is indicated during simple or complex dental extraction phases. Its intended purpose is to lift teeth or mobilize residual dental roots to facilitate their removal from the socket. Thanks to its curvature, it allows the practitioner to apply controlled leverage forces on the dental structures. It is particularly useful for breaking periodontal ligament fibers before final extraction. This Helmut Zepf instrument is therefore a major ally for managing fractured or deeply anchored roots.

What are the technical characteristics of the 17.007.07 elevator?

This instrument is distinguished by its ergonomic design and its manufacture from high-quality medical stainless steel. It belongs to the category of Class I manual instruments according to medical device regulations. Reference 17.007.07 corresponds to model number 7 of the X - Luxa range, characterized by a curved working end. This specific geometry is optimized for force transmission during luxation. Like all Helmut Zepf products, it is delivered non-sterile and requires a complete processing protocol before being put into service.

What are the contraindications for the use of this elevator?

The main medical contraindication identified by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If a hypersensitivity reaction is observed during the procedure, the procedure must be immediately stopped and necessary medical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any use of this surgical instrument.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to visually inspect the curved luxator for any damage such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn instrument is strictly prohibited. Although there is no defined maximum limit for processing cycles due to the quality of the materials, natural wear must be evaluated by the healthcare professional before each clinical act.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I, in accordance with the regulatory requirements in force for manual dental instruments. The manufacturer guarantees the traceability and quality of the stainless steel used. Safety instructions stipulate that the use of this tool is exclusively reserved for qualified healthcare professionals. Compliance with the cleaning and sterilization protocols defined by Helmut Zepf is mandatory to maintain the integrity of the device and patient safety.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.