Curette Tip. M4X0.5. - Helmut Zepf (24.751.103G) - 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: 24.751.103G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf M4X0.5 CURETTE TIP?
The Helmut Zepf curette tip, bearing reference 24.751.103G, is an interchangeable manual dental instrument equipped with an M4X0.5 thread. Manufactured by Helmut Zepf Medizintechnik GmbH, it is designed in high-quality medical stainless steel to ensure structural resistance during curettage procedures. This device belongs to Class I of medical devices. Its design allows for adaptation onto compatible handles, thus offering a modular solution for periodontology and conservative dentistry interventions. As a non-sterile instrument upon delivery, it requires a complete cleaning and sterilization protocol before its first use in a surgical practice.
What are the clinical indications for this instrument?
This manual instrument is primarily indicated for periodontology procedures. Its intended use includes the removal of subgingival tartar and root planing to eliminate infected cementum. In oral surgery, this curette tip is used for cleaning sockets after extraction or for the debridement of inflammatory tissues during flap surgeries. It allows practitioners to treat root surfaces with precise mechanical action, thereby promoting epithelial reattachment and the reduction of gingival inflammation. Its application is strictly reserved for qualified healthcare professionals mastering manual curettage techniques.
What are the technical characteristics of the 24.751.103G tip?
The Helmut Zepf curette tip is distinguished by its M4X0.5 technical thread, ensuring stable and secure fixation on compatible instrument handles in the range. Manufactured from medical stainless steel, it features cutting edges that must be inspected before each use. The manufacturer specifies that the product is delivered non-sterile and must undergo a complete reprocessing cycle (cleaning, disinfection, and sterilization). Due to its robust design and the materials used, there is no defined maximum limit of processing cycles, although the user must check for the absence of visible damage, such as cracks or excessive wear of the sharp edges, before any intervention.
What are the contraindications for the use of this curette?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Since the instrument is made of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the clinical act, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any manipulation. Additionally, the use of the instrument is prohibited if it shows visible defects such as breaks or blunt cutting edges.
What are the maintenance and sterilization precautions?
Helmut Zepf products must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to perform thorough cleaning to remove all organic debris before the sterilization phase. The practitioner must inspect each curette tip to detect any visible damage, particularly cracks or defects on the active parts. Any damaged or worn instrument must never be used. The reprocessing process must follow standard hospital or dental practice sterilization protocols, ensuring compatibility with other products used simultaneously during the decontamination chain.
Who is the manufacturer and what standards are respected?
The curette tip is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer guarantees the use of medical stainless steel compliant with health requirements for manual instruments. Although specific CE marking is not detailed in the source data, the product meets the safety and performance requirements for manual dental instruments. The use of this device is strictly reserved for healthcare professionals, and compliance with the manufacturer's safety and maintenance instructions is mandatory to ensure patient safety and instrument longevity.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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