Dental Curette - Helmut Zepf (41.855.04Z) - Delynov
The Curette - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.855.04Z.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf 41.855.04Z curette?
The Helmut Zepf curette, referenced under code 41.855.04Z, is a manual surgical instrument specifically developed for oral health professionals. Manufactured by Helmut Zepf Medizintechnik GmbH, it is designed in high-quality medical stainless steel. This device belongs to the instrument category (INSTRU) and is distinguished by its robust structure adapted to the requirements of dental operating blocks. As a Class I device, it meets the basic safety standards for non-invasive or invasive instruments for temporary use. Its configuration allows for a stable grip for precise curettage procedures.
What are the clinical indications?
The intended use for this Helmut Zepf instrument is that of a manual dental instrument. In clinical practice, it is indicated for cleaning surgical sites, removing inflammatory or granulation tissue, as well as for alveolar curettage following tooth extraction. Its use occurs mainly during periodontal or pre-implant surgeries where sanitation of the bone or gingival site is imperative. This device is exclusively reserved for healthcare professionals trained in oral surgery techniques, thus guaranteeing an application in accordance with current medical protocols.
What are the technical characteristics?
The Helmut Zepf 41.855.04Z curette is a non-sterile instrument upon delivery, requiring a complete reprocessing cycle before its first use. It is manufactured from medical stainless steel, a material chosen for its resistance to repeated sterilization cycles. The manufacturer, Helmut Zepf Medizintechnik GmbH, specifies that the design of the instrument and the materials used do not allow for the definition of a maximum limit of processing cycles, although the user must inspect the instrument for any cracks, breaks, or defects on the cutting edges before each use. Any visible wear must result in the immediate withdrawal of the product.
What are the contraindications for use?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken. It is therefore recommended to check the allergic history of patients before any manipulation. Furthermore, the use of an instrument showing visible damage (cracks, corrosion) is strictly prohibited to avoid any risk of intraoperative breakage.
What are the maintenance and sterilization precautions?
Like all products from Helmut Zepf Medizintechnik GmbH, this curette must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The reprocessing process must be complete to guarantee the asepsis of the device. Before sterilization, thorough cleaning is essential to remove any biological residue. It is also crucial to check compatibility with other cleaning or disinfection products used. The manufacturer emphasizes the importance of never using damaged or worn products, as defects on the cutting edges can compromise clinical efficacy and patient safety.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). The manufacturer ensures the traceability and compliance of the instrument with the regulatory requirements applicable to manual dental instruments. Compliance with the instructions for use and safety provided by Helmut Zepf is mandatory to maintain the performance of the device. As a professional instrument, it is subject to rigorous maintenance protocols under the responsibility of the practitioner.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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