LUCAS CURETTE FIG. 1 - Helmut Zepf (41.855.01Z)
Optimize your surgical curettage with the Helmut Zepf Lucas curette
Designed for precise handling during dental surgical procedures, this manual curette ensures efficient cleaning of tissues and dental structures.
- Use: Manual instrument for dental surgical treatment.
- Material: High-quality medical stainless steel.
- Ergonomics: Design adapted for meticulous work on dental structures.
- Safety: Class I medical device, delivered non-sterile and autoclavable.
Product features
The LUCAS. CURETTE.FIG. 1 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.855.01Z.
- Reserved for healthcare professionals. Read instructions carefully before use.
fabricant : HELMUT ZEPF Medizintechnik Gmbh , Obere Hauptstraße 16-22, D- 78606 Seitingen-Oberflacht BUT PRÉVU / INDICATION Instrument dentaire manuel utilisé pour travailler sur la dent / l'appareildentaire lors d'un traitement chirurgical. Les effets secondaires indésirables l'intolérance aux métaux chez le patient peut résulter d'un contact avec l'instrument, qui est en acier inoxydable médical une réaction d'hypersensibilité était toujours déclenchée devenir. la procédure doit être arrêtée si une telle réaction se produit et les mesures nécessaires sont prises en conséquence. consignes d'utilisation et de sécurité tous les instruments doivent être nettoyés avant d'être utilisés pour la première fois et compléter avant toute utilisation ultérieure nettoyé, désinfecté et stérilisé ! il est très important de nettoyer chaque produit avant utilisation dommages et usures visibles, par ex. b. fissures, cassures ou des défauts sur les arêtes de coupe. n'utilisez jamais de produits endommagés ou usés. les produits de helmut zepf medizintechnik gmbh sont livrés non stériles. les produits doivent être à l'avance nettoyé et stérilisé. la compatibilité aussi les autres produits doivent être vérifiés au préalable. retraitement en raison de la conception du produit, des matériaux utilisés et il ne peut y avoir de limite maximale définie pour l'utilisation prévue des cycles de traitement réalisables peuvent être déterminés.réservé aux professionnels de santé.
What is the Helmut Zepf LUCAS FIG. 1 curette?
The LUCAS FIG. 1 curette, referenced under code 41.855.01Z, is a high-precision manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This medical device is manufactured from high-quality medical stainless steel, ensuring the robustness necessary during surgical interventions. As an instrument in the INSTRU category, it features an ergonomic structure adapted to the requirements of practitioners for work on the tooth or dental apparatus. This product is delivered non-sterile by Helmut Zepf and requires a complete preparation protocol before any clinical use. Its specific design allows for precise handling during the curettage or tissue cleaning phases during oral surgery procedures.
What are the clinical indications for this instrument?
The LUCAS FIG. 1 curette is indicated as a manual dental instrument used specifically for working on the tooth or dental apparatus during surgical treatment. Its use is reserved for qualified healthcare professionals. It is primarily employed in dental surgeries requiring direct intervention on hard or soft tissues. The manufacturer Helmut Zepf specifies that this tool is essential for debridement steps or the elimination of pathological tissues during operative acts. The instrument must be inspected before each use to detect any visible damage, such as cracks or defects on the cutting edges, to ensure the effectiveness of the surgical gesture and patient safety.
What are the technical characteristics of the 41.855.01Z curette?
The LUCAS FIG. 1 curette (41.855.01Z) is characterized by its manufacture in medical stainless steel, a standard material for Class I surgical instrumentation. This manual device is designed to offer optimal durability, although the manufacturer does not define a maximum limit for processing cycles due to the nature of the materials used. Technical characteristics include cutting edges that must remain intact to ensure instrument performance. Helmut Zepf emphasizes the importance of checking for the absence of wear, breakage, or structural defects before any intervention. Compatibility with other products used during surgery must also be verified beforehand by the practitioner.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of the Helmut Zepf LUCAS curette concerns hypersensitivity to metals. Contact with the medical stainless steel instrument may cause undesirable side effects or intolerance reactions in certain sensitive patients. If a hypersensitivity reaction is triggered during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken accordingly. Furthermore, it is strictly forbidden to use damaged or worn products, presenting cracks or defects on the active parts, as this could compromise patient safety or the outcome of the surgical treatment.
What are the maintenance and reprocessing precautions?
Reprocessing the LUCAS FIG. 1 curette is a critical step because the device is delivered non-sterile. According to the manufacturer's safety instructions, all instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. Complete cleaning is indispensable before sterilization to eliminate any residue. The practitioner must perform a rigorous visual inspection to identify any sign of wear or damage. Due to the robust design and materials selected by Helmut Zepf Medizintechnik GmbH, there is no predefined maximum number of sterilization cycles, but the functionality of the instrument must be validated by the professional before each act.
Who is the manufacturer and what standards are met?
The LUCAS FIG. 1 curette is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer adheres to strict manufacturing protocols to guarantee the quality of its manual instrumentation intended for dental surgeons. Although specific CE marking is not detailed in the provided sources, the product meets the safety and performance requirements for its intended purpose in dental surgery. The use of this instrument is strictly reserved for trained healthcare professionals, thus ensuring an application compliant with international medical standards for Class I devices.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |