Curved Luxator 3mm Figure 3 - Helmut Zepf (17.006.03)

What is the 3mm Curved Luxator Figure 3 - Helmut Zepf?

The 3mm Curved Luxator Figure 3, referenced under code 17.006.03, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Made of medical stainless steel, this tool is specifically developed for oral surgery interventions requiring effective root luxation. Its curved configuration combined with a 3mm tip width allows access to ligament spaces with great maneuverability. As a Class I device, it meets the quality requirements for professional use in dental practices or hospital environments. This product is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient.

What are the clinical indications for this instrument?

The purchase of a surgical luxator like this Helmut Zepf model is indicated for the mobilization of teeth and roots during extractions. Its primary use lies in severing the ligament fibers of the periodontium. By inserting the 3mm curved tip into the periodontal space, the practitioner exerts controlled pressure to break the attachments and facilitate avulsion. It is particularly useful in cases of fractured roots or to prepare for a less invasive extraction. The instrument is exclusively reserved for qualified healthcare professionals mastering oral surgery and implantology techniques. Its curved design facilitates access to posterior areas or complex angulations where a straight instrument would be less effective.

What are the technical characteristics of the 17.006.03 luxator?

The Helmut Zepf 3mm curved luxator is distinguished by its manufacture in high-quality medical stainless steel, guaranteeing the necessary resistance to mechanical stress during luxation. Reference 17.006.03 corresponds to Figure 3 of the range, characterized by a specific curvature of the working part. The 3mm width is optimized to insert precisely into the sulcus. According to the manufacturer data from Helmut Zepf Medizintechnik GmbH, the instrument is a Class I medical device (Class Ir according to MDC0483). Its design does not allow for a defined maximum limit of processing cycles, but the user must imperatively check for the absence of visible damage, such as cracks or defects on the edges, before each intervention.

What are the contraindications for the use of this device?

The main 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 surgical act, the procedure must be immediately interrupted and the necessary medical measures must be taken. Furthermore, it is strictly forbidden to use an instrument showing signs of wear, cracks, or damaged cutting edges, as this could compromise patient safety and the effectiveness of the surgical gesture. Use is strictly limited to trained healthcare professionals.

What are the maintenance and sterilization precautions?

As Helmut Zepf Medizintechnik GmbH products are delivered non-sterile, a complete reprocessing cycle is mandatory before the first use. This includes cleaning, disinfection, and sterilization. It is crucial to clean each product individually to remove any residue before autoclaving. The manufacturer emphasizes the importance of checking compatibility with other cleaning or disinfection products used. Although no maximum limit of cycles is defined due to the robustness of the materials, the instrument must be visually inspected after each treatment. Any presence of breakage or structural defect requires the immediate removal of the device from the clinical circuit to ensure optimal safety during surgery.

Who is the manufacturer and what standards are respected?

The 3mm curved luxator is manufactured by Helmut Zepf Medizintechnik GmbH, headquartered in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with production standards for manual dental instruments. The device is classified as Class I (Class Ir according to the MDC0483 nomenclature), which confirms its status as a regulated medical device. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to maintain the integrity of the instrument and ensure patient protection. This manufacturer's expertise in working with medical stainless steel guarantees a reliable tool for the daily requirements of dental and implant surgery, subject to maintenance in accordance with technical guidelines.

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