Curved 5mm Luxator - Helmut Zepf (17.006.04)

What is the curved luxator 5mm figure 4 - Helmut Zepf?

The curved luxator 5mm figure 4, referenced under code 17.006.04, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this tool is characterized by a curved working end with a width of 5mm. It belongs to the category of consumables for dental surgery and is classified as a Class I medical device. Its robust structure meets the requirements of daily interventions in the dental practice, while ensuring handling adapted to the needs of dental surgeons and implantologists.

What are the clinical indications for this device?

This instrument is specifically indicated for the luxation of teeth and roots. Within the framework of oral and implant surgery, its primary role is to rupture the ligament fibers of the periodontium. The use of a curved luxator is particularly relevant for accessing difficult areas where a straight instrument would not allow for an optimal angle of attack. By inserting the 5mm blade into the alveolar-dental space, the practitioner can mobilize the tooth before the actual extraction, thus contributing to the preservation of surrounding bone structures.

What are the technical characteristics of the luxator 17.006.04?

The Helmut Zepf luxator model 17.006.04 features a figure 4 tip with a width of 5mm. Its specific curvature is designed to follow the root anatomy during luxation maneuvers. Manufactured in medical stainless steel, it is built to withstand mechanical stresses exerted during extractions. The device is delivered non-sterile and requires a complete protocol of cleaning, disinfection, and sterilization before its first use and between each patient. Its design allows for a number of processing cycles not defined by a maximum limit, subject to a visual inspection of its integrity.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, specifically the medical stainless steel used for manufacturing. If an allergic reaction or hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any intervention using this luxator.

What are the maintenance and safety precautions?

Before each use, the practitioner must imperatively check for the absence of visible damage such as cracks, breaks, or defects on the cutting edges. It is strictly forbidden to use damaged or worn products. As the luxator is delivered non-sterile, it must undergo a complete reprocessing cycle (cleaning, disinfection, and sterilization). Compatibility with other products used simultaneously must also be verified beforehand. This device is exclusively reserved for professional use by qualified healthcare practitioners in dental surgery.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Germany. This curved luxator is a Class I medical device compliant with the regulatory requirements in force for manual dental instruments. Although specific CE marking is not detailed in the source data, the product meets manufacturing standards for medical stainless steel. Traceability is ensured by the technical reference 17.006.04, allowing professionals to buy this curved luxator with the assurance of equipment compliant with clinical reprocessing protocols.

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