Lucas Curette - Helmut Zepf (41.855.00Z) - Delynov
The Curette Lucas - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.855.00Z.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Lucas curette?
The Lucas curette (reference 41.855.00Z) is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this curette is an essential tool in oral surgery for the treatment of hard and soft tissues. Its double-ended structure allows the practitioner to intervene effectively in alveolar areas. This device belongs to Class I of medical devices, ensuring compliance with regulatory requirements for reusable surgical instruments. It is delivered non-sterile and requires a complete cleaning and sterilization protocol before each use to ensure patient safety.
What are the clinical indications for this instrument?
The Lucas curette is primarily indicated for oral surgery procedures requiring thorough cleaning of bone cavities. It is commonly used for alveolar curettage after tooth extraction to remove debris, granulation tissue, or infected tissue. It is also employed for the enucleation of periapical cysts and debridement during periodontal or pre-implant surgeries. By working directly on the tooth or dental apparatus, this Helmut Zepf instrument allows for optimal preparation of the surgical site, thus promoting healthy healing and limiting the risks of post-operative complications related to the persistence of pathogenic tissues.
What are the technical characteristics of reference 41.855.00Z?
Reference 41.855.00Z corresponds to a Lucas curette from the Helmut Zepf range, characterized by an ergonomic design adapted to the requirements of fine surgery. Although specific dimensions are not detailed beyond the product code, this type of instrument is distinguished by its spoon-shaped working ends, optimized for scraping and tissue extraction. Manufactured by Helmut Zepf Medizintechnik GmbH, it benefits from a robust construction in medical stainless steel. As a Class I device, it meets industrial manufacturing standards for manual surgical instruments, offering the necessary resistance to repeated decontamination and autoclave sterilization cycles.
What are the contraindications for using the Lucas curette?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns patients with known hypersensitivity or intolerance to metals. As the instrument is manufactured from medical stainless steel, contact may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any use. Additionally, the use of the instrument is strictly reserved for qualified healthcare professionals mastering dental and oral surgery techniques.
What are the maintenance and reprocessing precautions?
Like any surgical instrument from the Helmut Zepf brand, the Lucas curette must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The practitioner must visually inspect the instrument to detect any damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is prohibited to guarantee the effectiveness of the procedure and patient safety. Due to its design and the materials used, there is no defined maximum limit of treatment cycles, but natural wear must be monitored. Compatibility with other cleaning and sterilization products must also be verified beforehand.
Who is the manufacturer and what standards are respected?
The Lucas curette 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 (MDC0483). The manufacturer complies with strict safety and quality protocols for the production of manual surgical instruments. Each product is delivered non-sterile, leaving the responsibility for final reprocessing to the healthcare professional. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to maintain the integrity of the instrument and ensure its compliance during surgical interventions on the dental apparatus.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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