Right Luxator 5mm Imaging Fig.2 - Helmut Zepf (17.006.02) - Delynov

What is the 5mm straight luxator imaging fig.2?

The 5mm straight luxator imaging fig.2, referenced under code 17.006.02, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this device is intended for the luxation of roots and teeth during extractions. Its straight structure and 5mm working part allow for effective insertion into the periodontal space. This product belongs to the category of reusable consumables (CONSO) and requires a complete cleaning and sterilization protocol before each use to ensure the safety of the patient and the practitioner.

What are the clinical indications?

This straight luxator is indicated for oral surgery and dental extraction. Its primary role is to facilitate avulsion by cutting ligament attachments and widening the socket. The use of a 5mm dental luxator is particularly recommended before the application of forceps to reduce the risk of root fracture. It is used with axial pressure and slight rotation movements to separate the tooth from its bony support. This instrument is reserved exclusively for qualified healthcare professionals practicing dentistry or maxillofacial surgery.

What are the technical characteristics?

The 5mm straight luxator Helmut Zepf features an ergonomic fig.2 configuration adapted for direct access. Manufactured from medical grade stainless steel, it is designed to withstand mechanical stress during luxation. The manufacturer, Helmut Zepf Medizintechnik GmbH, delivers this product non-sterile, requiring a complete processing cycle (cleaning, disinfection, and sterilization) before the first use. Reference code 17.006.02 allows for precise identification of the model. The 5mm width of the tip is calibrated to adapt to the standard anatomical dimensions of alveolar sites.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals, particularly the medical stainless steel used for the manufacture of the instrument. In the event of an allergic reaction or sign of hypersensitivity triggered during contact with the patient, the clinical procedure must be immediately interrupted. Appropriate medical measures must then be taken. It is also forbidden to use the instrument if it shows visible damage such as cracks, breaks, or defects on the cutting edges.

What are the maintenance and safety precautions?

Like any Class I instrument, the luxator must be subject to a rigorous inspection before each use. It is imperative to check for the absence of wear or deformations on the 5mm tip. Helmut Zepf products must be cleaned, disinfected, and sterilized before each cycle. Due to the design and materials, there is no defined maximum limit for processing cycles, but the user must discard any instrument showing signs of mechanical fatigue. Compatibility with other cleaning and sterilization products must be verified beforehand by the practice.

Who is the manufacturer and what standards are respected?

The official manufacturer is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. It meets the quality requirements for manual stainless steel dental instruments. Compliance with reprocessing protocols is essential, as the instruments are delivered non-sterile. As a recognized manufacturer, Helmut Zepf guarantees a product adapted to the requirements of modern dental surgery, subject to use in accordance with the provided safety and maintenance instructions.

State of the art

Surgical medical consumables play a decisive role in operative safety.