CURETTE TIP, M4X0.5 - Helmut Zepf (24.751.112GM5) - Delynov

What is the Helmut Zepf CURETTE TIP?

The Helmut Zepf CURETTE TIP, referenced under code 24.751.112GM5, is a manual instrumentation component designed for periodontal care. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this interchangeable tip features an M4X0.5 thread allowing secure attachment to the brand's compatible instrument handles. Its structure is specifically designed to meet the requirements of oral surgery and periodontology, providing a precise working interface for the treatment of tooth and root surfaces.

What are the clinical indications?

This manual instrument is indicated for prophylaxis and periodontal therapy procedures. It is primarily used by dental surgeons for the removal of subgingival calculus deposits and root planing. As a Gracey curette tip, it allows access to specific anatomical areas to remove infected cementum and smooth roots. Its use also extends to peri-implant maintenance and site preparation during more invasive periodontal surgeries, ensuring thorough cleaning of hard structures.

What are the technical specifications?

The Helmut Zepf curette tip is distinguished by its technical reference 24.751.112GM5 and its standardized M4X0.5 thread. Designed in medical grade stainless steel, it ensures mechanical resistance adapted to curettage forces. This device belongs to Class I of medical devices. The interchangeable design allows practitioners to replace only the working part, thus optimizing instrument inventory management. The quality of the steel used maintains an effective sharp edge for demanding periodontal debridement procedures.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance of the patient to metals, particularly medical stainless steel. An allergic reaction may be triggered upon contact of the instrument with the tissues. If such a reaction occurs during the procedure, the intervention must be immediately interrupted and necessary clinical measures must be taken. It is therefore imperative to check the patient's allergic history before any use of this manual instrument in the mouth.

What are the maintenance and sterilization precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and require a complete reprocessing cycle before the first use and after each subsequent use. The protocol includes cleaning, disinfection, and sterilization. The practitioner must visually inspect each tip before use to detect any damage such as cracks, breaks, or defects on the cutting edges. The use of worn or damaged instruments is strictly prohibited to ensure patient safety and the effectiveness of the surgical procedure.

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 medical device is classified as Class I according to current regulations (Class Ir - MDC0483 mentioned for reprocessing). The manufacturer emphasizes that the use of this instrument is exclusively reserved for qualified healthcare professionals. Compliance with German manufacturing standards ensures traceability and material quality meeting the strict requirements of modern dental and periodontal surgery.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.