Curette Tip M4X0.5 - Helmut Zepf (24.751.102LC)
The Pointe de Curette M4X0.5 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.102LC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf (24.751.102LC) curette tip?
The curette tip referenced 24.751.102LC is an interchangeable manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. It is designed in medical-grade stainless steel to meet the requirements of surgical interventions in the oral environment. This device is characterized by a specific M4X0.5 thread, allowing its fixation on suitable instrument handles. As an instrument in the INSTRU category, it is part of a modular approach for the practitioner, facilitating the replacement of the active end without changing the entire instrument. Its structure is designed to ensure the transmission of forces during curettage movements.
What are the clinical indications for this instrument?
This manual dental instrument is primarily indicated for oral surgery, periodontology, and implantology procedures. Its intended use concerns the cleaning of sockets after extraction, the removal of granulation tissue, or the debridement of inflammatory sites. The Helmut Zepf tip allows for targeted intervention on soft tissues and superficial bone structures. It is intended exclusively for qualified healthcare professionals who have mastered oral surgery protocols. Its use generally occurs during the preparation of a site before implant placement or to sanitize an infected area, thus ensuring an optimal surgical environment for healing.
What are the technical characteristics of the 24.751.102LC tip?
The major technical characteristic of this curette tip lies in its M4X0.5 connection system, ensuring strict compatibility with handles in the Helmut Zepf range using this screw pitch. Manufactured from medical stainless steel, it possesses mechanical resistance properties adapted to the constraints of dental surgery. The device is delivered non-sterile, which requires a strict processing protocol before the first use and between each patient. The dimensions and geometry of the working part are optimized for access to narrow areas of the oral cavity. It is imperative to check for the absence of visible damage, such as cracks or defects on the cutting edges, before any intervention.
What are the contraindications for the use of this device?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals, and more particularly to the components of medical stainless steel. If an allergic reaction or hypersensitivity reaction occurs in the patient during contact with the instrument, the surgical procedure must be immediately interrupted. Necessary corrective measures must then be taken accordingly. Furthermore, the use of this instrument is prohibited if the device shows visible signs of wear, breakage, or blunt cutting edges, as this could compromise patient safety and the effectiveness of the surgical procedure.
What are the maintenance and reprocessing precautions?
Like all Helmut Zepf Medizintechnik GmbH products, this curette tip is delivered non-sterile. It must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. The manufacturer specifies that due to the design and materials used, it is not possible to define a maximum limit of treatment cycles, provided that the instrument shows no functional degradation. The practitioner must carefully inspect the tip before each use to detect any cracks or defects. Compatibility with other products and cleaning solutions used must also be verified beforehand to preserve the integrity of the stainless steel.
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 product is classified as a Class I medical device (Class Ir according to reprocessing mentions). It meets the regulatory requirements for manual dental instruments. Manufacturing is based on the use of medical stainless steel compliant with industry standards for invasive surgical devices. As a recognized manufacturer, Helmut Zepf ensures the traceability of its instruments through precise technical references, such as code 24.751.102LC, thus guaranteeing healthcare professionals reliable equipment that complies with current safety standards for the practice of dental surgery.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |



