Zepf Limes for Periodontology - Helmut Zepf (24.488.02) - Delynov

What is the Helmut Zepf 24.488.02 periodontal file?

The periodontal file referenced 24.488.02 is a specific manual instrument developed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this file is designed for precision interventions on the hard tissues of the tooth. It belongs to the category of technical consumables for periodontology. Its structure is optimized to meet the requirements of dental surgeons during the root cleaning and smoothing phases. As a Class I device, it meets the rigorous manufacturing standards imposed for non-invasive or short-term invasive manual surgical instruments, ensuring reliable integration into the dental practice's technical platform.

What are the clinical indications for this instrument?

This periodontal file is indicated for the mechanical treatment of root surfaces. In periodontal surgery, it is used for the removal of stubborn subgingival tartar deposits and for the smoothing of altered cementum. Its use is particularly relevant during flap procedures or open curettage, where precise finishing of the root is necessary to promote epithelial reattachment. The Helmut Zepf instrument allows access to complex anatomical areas where standard curettes may be limited. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery and periodontology techniques.

What are the technical characteristics of the 24.488.02 file?

The Helmut Zepf periodontal file is characterized by its medical stainless steel composition, a material chosen for its resistance to sterilization cycles and its durability in a clinical environment. The reference code 24.488.02 identifies a specific working geometry unique to the Helmut Zepf Medizintechnik GmbH range. The instrument is delivered non-sterile, which requires a strict preparation protocol before the first use. The design of the cutting edge is engineered to provide consistent efficiency when removing mineralized deposits. No maximum cycle of use is defined by the manufacturer; the integrity of the instrument must be visually verified by the practitioner before each intervention.

What are the contraindications for the use of this file?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the operative act, the procedure must be immediately stopped and the necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, in order to avoid any risk of tissue lesion or in vivo rupture.

What are the maintenance and reprocessing precautions?

Like any Helmut Zepf instrument, this file must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The reprocessing process must be complete to guarantee the safety of the patient and the practitioner. It is crucial to check for the absence of wear or damage before each cycle. Due to its design and the materials used, there is no defined maximum limit for treatment cycles, but the use of damaged or worn products is formally prohibited. Compatibility with other products and cleaning solutions must also be verified beforehand to preserve the surface condition of the stainless steel.

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 device is classified as Class I according to the regulations in force on medical devices. The manufacturer ensures the traceability and compliance of the instrument with the safety requirements for manual dental instruments. Although CE marking specifications are not detailed in the source data, compliance with cleaning and sterilization protocols is a central requirement of the manufacturer to maintain product compliance during clinical use. The product is exclusively intended for professional use by dental health experts.

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