Curette Tip, M4x0.5 - Helmut Zepf (24.751.112GM5OX) - Delynov

What is the Helmut Zepf curette tip?

The Helmut Zepf curette tip, referenced under code 24.751.112GM5OX, is a manual instrumentation component intended for oral surgery. Manufactured from medical stainless steel, this tip features a specific M4x0.5 thread for assembly. It belongs to the category of rotary or manual instruments of the curette insert type, designed by Helmut Zepf Medizintechnik GmbH to meet clinical practice requirements. Its structure is engineered to allow precise access to surgical areas while ensuring the necessary robustness for curettage maneuvers.

What are the clinical indications for this curette insert?

This instrument is indicated as a manual dental instrument for various oral surgery procedures. Its primary use involves soft tissue debridement, cleaning sockets after extraction, or treating root surfaces during periodontal surgeries. As a curette insert, it allows the practitioner to precisely remove granulation tissue or calcified deposits. Its use is strictly reserved for qualified healthcare professionals within the framework of odontological or implant care requiring reliable manual instrumentation.

What are the technical characteristics of this device?

The Helmut Zepf curette tip is distinguished by its M4x0.5 precision thread, ensuring a stable connection with compatible instrument handles. Manufactured by Helmut Zepf Medizintechnik GmbH, it is designed in high-quality medical stainless steel. This device is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. Its durability is not limited by a predefined number of cycles but depends on the practitioner's visual inspection to detect any signs of wear, cracks, or defects on the cutting edges.

What are the contraindications for using this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the procedure, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any use of this curette insert in the mouth.

What are the maintenance and reprocessing precautions?

As a non-resorbable and reusable instrument, this curette insert requires a rigorous reprocessing protocol. Before each use, the instrument must be cleaned, disinfected, and sterilized according to current standards. The practitioner must check for the absence of visible damage such as cracks, breaks, or loss of sharpness on the cutting edges. The use of damaged or worn products is prohibited. Due to its design and the materials used, there is no defined maximum limit of treatment cycles; the decision to decommission the device rests with the professional after inspection.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. This product is classified as a Class I medical device (Class Ir according to the reference text). In accordance with regulations, it meets the safety and performance requirements for manual instruments. Traceability is ensured by the technical reference 24.751.112GM5OX. Professionals must refer to the manufacturer's instructions for cleaning and sterilization to guarantee the device's compliance during use in dental offices or operating rooms.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.