CURETTE TIP, M4X0.5 - Helmut Zepf (24.751.114GM5) - Delynov
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: 24.751.114GM5.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 24.751.114GM5 curette tip?
The Helmut Zepf curette tip, referenced under code 24.751.114GM5, is a manual instrumentation component designed for specialized dental care. Manufactured in medical-grade stainless steel by Helmut Zepf Medizintechnik GmbH, this tip features an M4X0.5 thread allowing it to be adapted onto compatible handles. Its structure is specifically designed to provide a precise tactile response during the removal of subgingival deposits and the treatment of root surfaces. As a Class I instrument, it meets the safety requirements for non-invasive or short-term invasive medical devices used in dental practices.
What are the clinical indications for this instrument?
This manual instrument is primarily indicated for periodontology and prophylactic hygiene procedures. It is used by dental surgeons and implantologists for root planing, deep tartar removal, and cleaning of surgical sites during flap surgeries. Its morphology allows access to root irregularities and the treatment of inflammatory soft tissues. The intended use by the manufacturer Helmut Zepf is that of a versatile manual dental instrument, essential for maintaining the integrity of the tooth's supporting tissues and preventing peri-implantitis through rigorous mechanical debridement.
What are the technical characteristics of the 24.751.114GM5 tip?
The Helmut Zepf curette tip is distinguished by its M4X0.5 technical thread, guaranteeing stable and secure fixation on the instrument-holding handle. Designed in medical stainless steel, it possesses mechanical properties suitable for cutting and scraping mineralized tissues without risk of breakage under normal stress. The device is delivered non-sterile, which requires a rigorous preparation protocol before the first use in the mouth. Its design allows for complete reprocessing, including cleaning, disinfection, and sterilization in an autoclave, thus ensuring longevity in compliance with modern clinical practice standards in oral surgery.
What are the contraindications for using this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with an allergic patient may trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and appropriate medical measures must be taken. It is therefore imperative to check the patient's allergic history before any use. Furthermore, use is strictly reserved for qualified healthcare professionals proficient in manual instrumentation techniques.
What are the maintenance and reprocessing precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use and after each subsequent use. Before any intervention, the practitioner must perform a thorough visual inspection to detect potential damage or signs of wear such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to guarantee patient safety. Due to the quality of the materials used by Helmut Zepf, there is no defined maximum limit of treatment cycles, but compatibility with other cleaning products and sterilization devices must be verified beforehand.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to associated MDR mentions). It complies with regulatory requirements for manual dental instruments. The manufacturer emphasizes that its products are delivered non-sterile and must undergo a full reprocessing cycle (cleaning and sterilization) before use. Traceability is ensured by the technical reference 24.751.114GM5, allowing for precise identification of the batch and technical specifications within the Helmut Zepf instrumentation range.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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