Pointed Curette M4X0.5 - Helmut Zepf (24.751.123L)
The Curette Pointée 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: 24.751.123L.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 24.751.123L pointed curette?
The pointed curette referenced 24.751.123L is a manual surgical instrument developed by Helmut Zepf Medizintechnik GmbH. This device belongs to the category of oral surgery instruments and is distinguished by its M4X0.5 thread, allowing its integration onto compatible handles from the range. Manufactured from medical stainless steel, this curette is designed to offer optimal resistance during clinical manipulations. As a Class I device, it meets the quality requirements for non-invasive or short-term invasive tools used in dental practices. It is delivered non-sterile and requires a complete preparation protocol before its first use.
What are the clinical indications for this instrument?
This instrument is indicated for dental and oral surgery procedures requiring meticulous tissue cleaning. The Helmut Zepf pointed curette is mainly used for the removal of granulation tissue, alveolar curettage after extraction, or cleaning bone defects before guided bone regeneration. Its specific shape allows the practitioner to intervene with precision in interproximal spaces or difficult-to-access areas. It is exclusively reserved for use by qualified healthcare professionals, thus guaranteeing an application compliant with current clinical protocols in implantology and periodontology.
What are the technical characteristics of the 24.751.123L curette?
The Helmut Zepf 24.751.123L curette is characterized by a pointed working end and an M4X0.5 fixation system. This standardized thread from the manufacturer allows interchangeability with various ergonomic handles. Its medical stainless steel structure ensures compatibility with repeated sterilization cycles. Given the design of the instrument and the materials used, there is no defined maximum limit of processing cycles, although the user must inspect the device before each use to detect any visible damage such as cracks or defects on the cutting edges.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this Helmut Zepf curette is the patient's known hypersensitivity or intolerance to metals, specifically to medical stainless steel. A hypersensitivity reaction can be triggered upon contact between the instrument and the tissues. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any manipulation. Furthermore, the use of an instrument showing signs of wear, breakage, or damaged edges is strictly prohibited.
What are the maintenance and reprocessing precautions?
Helmut Zepf products are delivered non-sterile. It is imperative to perform complete cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. The reprocessing process must follow standard hospital or dental practice sterilization protocols for stainless steel devices. Before each cycle, the instrument must be visually inspected: any sign of corrosion, crack, or deformation must lead to the immediate disposal of the curette. Compatibility with other cleaning products or other handles must also be verified beforehand by the professional.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing mentions). The manufacturer ensures compliance with the regulatory requirements applicable to manual dental instruments. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to guarantee the longevity of the tool and patient safety. As a Class I device, it is designed to meet dental industry standards for reusable tools after sterilization.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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