Special Zepf-Bionik Curette, dentist surgeon, bone graft and maxillofacial surgery (24.204.11G) - Delynov
The Curette spéciale Zepf-Bionik , chirurgien-dentiste, greffe osseuse et chirurgie maxillo-faciale is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reference: 24.204.11G.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Zepf-Bionik special curette (24.204.11G)?
The Zepf-Bionik special curette, referenced under code 24.204.11G at Delynov, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Distributed under the brand Helmut Zepf, it is designed in medical stainless steel to meet the requirements of oral surgery. This instrument presents itself as a robust solution for practitioners performing complex interventions. Its structure is specifically adapted for the manipulation of hard and soft tissues in a demanding surgical environment. As a Class I device, it complies with the rigorous manufacturing standards imposed on reusable surgical instruments.
What are the clinical indications for this instrument?
This bone surgery curette is primarily indicated for bone grafting and maxillofacial surgery procedures. It allows the surgeon to perform socket cleaning, removal of inflammatory or granulation tissue, as well as the preparation of bone sites before implantation. Its use is common in bone reconstruction protocols where a bone graft curette is necessary to manipulate filling materials or to smooth bone surfaces. It is exclusively reserved for use by qualified healthcare professionals in the fields of dentistry and orofacial surgery.
What are the technical characteristics of the 24.204.11G curette?
The Zepf-Bionik special curette is characterized by its medical stainless steel construction, ensuring resistance to repeated cleaning and sterilization processes. This device from the brand Helmut Zepf is delivered non-sterile and must imperatively undergo a complete decontamination cycle before its first use and after each intervention. The manufacturer emphasizes the importance of checking the integrity of the instrument, particularly the absence of cracks, breaks, or defects on the cutting edges before any manipulation. Its ergonomic design is intended to offer optimal control during curettage procedures in maxillofacial surgery.
What are the contraindications for the use of this curette?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or metal intolerance in the patient. Since the instrument is composed of medical stainless steel, contact may trigger an allergic reaction. 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 crucial to validate the patient's anamnesis regarding potential allergies to metallic components before any use of this device from the brand Helmut Zepf.
What are the maintenance and reprocessing precautions?
Like any reusable Class I surgical instrument, this curette requires a strict protocol. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit of treatment cycles, as long as the instrument does not show visible damage. The user must meticulously inspect the tool to detect any wear, corrosion, or deformation. The use of damaged or worn products is strictly prohibited to guarantee patient safety and the effectiveness of the surgical procedure.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Germany. This medical device belongs to Class I (Class Ir according to the reprocessing mentions). It is marketed by Delynov under the brand Helmut Zepf. Compliance with regulatory requirements is ensured by adherence to Helmut Zepf's manufacturing protocols, guaranteeing an instrument adapted to maxillofacial surgery. Although the specific CE marking is not detailed in the source data, the product follows the directives relating to manual reusable medical devices, including the cleaning and sterilization obligations provided by the manufacturer.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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