CURETTE TIP, M4X0.5 - Helmut Zepf (24.751.114MC) - Delynov

What is the Helmut Zepf curette tip?

The Helmut Zepf curette tip, referenced under code 24.751.114MC, is an interchangeable manual dental instrument featuring an M4X0.5 thread. Manufactured by Helmut Zepf Medizintechnik GmbH, it is designed in high-quality medical stainless steel to meet the requirements of intraoral interventions. This device belongs to the category of manual diagnostic and treatment instruments, offering a structure adapted for precision movements during root surface cleaning or the removal of infected tissue.

What are the clinical indications?

This instrument is primarily indicated as a manual dental instrument for periodontology and oral surgery procedures. Its intended use is for the removal of subgingival calculus, root planing, and soft tissue curettage during flap surgeries or periodontal pocket treatments. It is used by healthcare professionals to debride surgical sites and prepare surfaces before tissue regeneration or implant placement, thereby ensuring an environment conducive to healing.

What are the technical characteristics?

The curette tip is distinguished by its technical reference 24.751.114MC and its M4X0.5 threaded fixation system, allowing compatibility with suitable instrument handles. It is manufactured from medical stainless steel, a material chosen for its corrosion resistance and its ability to maintain an effective cutting edge. As a Class I device, this instrument must undergo rigorous inspection before each use to detect potential visible damage such as cracks, breaks, or defects on the cutting edges.

What are the contraindications for use?

The main contraindication identified by the manufacturer Helmut Zepf concerns the patient's known hypersensitivity or intolerance to metals, specifically the medical stainless steel used in the instrument's composition. If an allergic reaction or hypersensitivity manifests during the intervention, the procedure must be stopped immediately and necessary clinical measures must be taken. It is therefore imperative to check the patient's allergic history before any contact with the instrument.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use as well as after each subsequent use. The reprocessing process must be complete to ensure patient safety. Due to the instrument's design and the materials used, there is no defined maximum limit of processing cycles, but the user must check compatibility with other products and the absence of wear. Any damaged instrument or one showing visible defects must be discarded.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as a Class I instrument (Class Ir according to the raw MDR text) in accordance with European medical device regulations. Compliance with cleaning and sterilization protocols is essential to maintain conformity with hospital hygiene standards. The use of this instrument is strictly reserved for healthcare professionals qualified in dental and oral surgery.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.