Curette Tip, M4x0.5 - Helmut Zepf (24.751.114G) - 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: 24.751.114G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 24.751.114G curette tip?
The curette tip referenced 24.751.114G is a manual instrumentation component manufactured by Helmut Zepf Medizintechnik GmbH. This device is designed in medical stainless steel, a standard material for surgical instrumentation due to its mechanical properties. This specific model features an M4X0.5 thread, allowing it to be mounted on interchangeable instrument handles. As a manual instrument, it is intended for precise curettage and cleaning tasks within the oral cavity. This device belongs to Class I medical devices, ensuring its compliance with basic regulatory requirements for non-invasive or invasive instruments for temporary use.
What are the clinical indications for this instrument?
This manual instrument is primarily indicated for periodontology and oral surgery procedures. Its intended use includes mechanical removal of subgingival calculus, root planing to eliminate infected cementum, and curettage of granulation tissue during alveolar surgeries. Practitioners use this Helmut Zepf curette tip to debride surgical sites or treat periodontitis. It allows access to complex anatomical areas to ensure effective mechanical decontamination. Use is strictly reserved for qualified healthcare professionals mastering manual curettage techniques in a sterile environment.
What are the technical characteristics of the 24.751.114G tip?
The curette tip is characterized by its M4X0.5 type threaded connection, ensuring stable fixation on compatible handles from the Helmut Zepf range. Manufactured from medical stainless steel, it features cutting edges designed for clinical efficiency. The manufacturer delivers this product non-sterile, which requires a complete preparation protocol before any use. Before each intervention, the practitioner must imperatively inspect the instrument to detect any visible damage such as cracks, breaks, or excessive wear of the sharp edges. Using a damaged product is prohibited to ensure patient safety and the effectiveness of the surgical procedure.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient's tissues may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the operative act, the procedure must be immediately interrupted and necessary medical measures must be initiated. It is the practitioner's responsibility to check the patient's allergic history before the intervention. Furthermore, the use of the instrument is contraindicated if it shows structural defects or visible corrosion after reprocessing cycles.
What are the maintenance and sterilization precautions?
Like all instruments from the Helmut Zepf Medizintechnik GmbH brand, this curette tip must follow a rigorous cycle of cleaning, disinfection, and sterilization before the first use and after each subsequent use. Reprocessing must be complete to ensure device asepsis. Although the design and materials used do not define a strict maximum limit of treatment cycles, the longevity of the instrument depends on maintenance and compliance with sterilization protocols. It is crucial to carefully clean the M4X0.5 thread to guarantee the durability of the mechanical connection. Any instrument showing signs of wear or dull cutting edges must be removed from service.
Who is the manufacturer and what standards are met?
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 according to current regulations. The manufacturer specifies that the instrument is delivered non-sterile and must be processed in accordance with the provided safety and usage instructions. Compliance with cleaning and sterilization protocols is the responsibility of the healthcare professional. Compatibility with other products and accessories must also be verified by the user before the intervention to ensure the proper functioning of the mechanical assembly during dental care.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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