M4X0.5 Curette Tip - Helmut Zepf (24.751.102G) - Delynov

What is the Helmut Zepf M4X0.5 curette tip?

The M4X0.5 curette tip, referenced under code 24.751.102G by the manufacturer Helmut Zepf, is an interchangeable manual dental instrumentation component. Manufactured from medical grade stainless steel, this tip is designed to be mounted on handles equipped with an M4X0.5 metric thread. This system allows practitioners to modulate their instrumentation according to the specific needs of each procedure while maintaining a rigid and reliable structure. This product belongs to the category of manual dynamic instruments used for the treatment of dental and bone surfaces.

What are the clinical indications for this instrument?

This Helmut Zepf curette tip is primarily indicated for periodontology and oral surgery procedures. It is used for the removal of subgingival calculus, root planing, and the elimination of granulation tissue in periodontal pockets. In implant or extraction surgery, it allows for thorough cleaning of the socket (alveolar curettage) to promote optimal healing. Its use is strictly reserved for qualified healthcare professionals proficient in manual curettage techniques.

What are the technical specifications of reference 24.751.102G?

Technical reference 24.751.102G is distinguished by its M4X0.5 screw connection system, guaranteeing precise compatibility with handles in the Helmut Zepf range. The instrument is designed in medical stainless steel, a material chosen for its corrosion resistance and its ability to maintain an effective cutting edge after several sterilization cycles. The product is delivered non-sterile and must undergo a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient.

What are the contraindications for the use of this curette tip?

The main medical contraindication is known hypersensitivity or intolerance of the patient to metals, specifically stainless steel. In the event of an allergic reaction or signs of hypersensitivity triggered during contact with the instrument, the clinical procedure must be immediately interrupted and necessary corrective measures applied. It is also contraindicated to use this instrument if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety.

What are the maintenance and reprocessing precautions?

Like any Helmut Zepf instrument, this tip must be cleaned, disinfected, and sterilized before each use. It is crucial to visually inspect the product for any wear or corrosion before use. Due to its design and the materials used, there is no defined maximum limit of processing cycles, but the user must verify compatibility with other products and ensure that the cutting edge remains functional. The use of damaged or worn products is strictly prohibited to guarantee the integrity of the treated tissues.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Germany. This medical device is classified as a Class I instrument according to current regulations. The manufacturer imposes strict reprocessing protocols to maintain the compliance and safety of the instrument. As a Class I device, it meets the safety and performance requirements for non-invasive or invasive manual surgical instruments for temporary use, intended exclusively for use by healthcare professionals.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.