Root Canal Spreader - Helmut Zepf (19.512.16) - Delynov
The Fouloir de Canal Radiculaire Luks - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.512.16.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Luks root canal plugger?
The Luks root canal plugger, bearing reference 19.512.16, is a precision manual instrument designed by Helmut Zepf. Manufactured from medical stainless steel, this device is specifically structured for endodontic procedures. Its design allows for rigorous handling during the compaction stages of filling materials. As an instrument from the Helmut Zepf Medizintechnik GmbH brand, it meets the quality requirements of practitioners for conservative care. This device belongs to the category of consumables reusable after a strict sterilization protocol, thus guaranteeing constant safety of use within the dental practice.
What are the clinical indications for this instrument?
This instrument is indicated for root canal treatment procedures, specifically for hot or cold vertical condensation of gutta-percha. Its role is crucial in ensuring that the filling material hermetically fills the canal system, including accessory canals, in order to prevent any bacterial reinfection. It is used by dental surgeons and endodontists during the final phases of endodontic therapy. The use of this Helmut Zepf Luks plugger is part of a care protocol aimed at preserving the tooth on the arch by ensuring a stable and precise three-dimensional filling.
What are the technical characteristics of the 19.512.16 plugger?
The Helmut Zepf Luks plugger (reference 19.512.16) is characterized by its manufacture from high-quality medical stainless steel. It is designed to withstand repeated cycles of cleaning, disinfection, and sterilization. This device is delivered non-sterile and must undergo a complete reprocessing before its first use and between each patient. The design of the instrument does not define a maximum limit of treatment cycles, as this depends on visible wear and the structural integrity of the steel. Any sign of cracks, breaks, or defects on the instrument must lead to its immediate removal from service to guarantee operative safety.
What are the contraindications for the use of this device?
The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, an allergic reaction may occur in certain sensitive patients. If a hypersensitivity reaction is triggered during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. It is therefore recommended to question the patient about their history of allergies to metallic components before any manipulation. Apart from this specificity related to the material, use is reserved exclusively for qualified healthcare professionals mastering endodontic techniques.
What are the maintenance and sterilization precautions?
Like any Helmut Zepf manual instrument, this plugger must be cleaned, disinfected, and sterilized before each use. The manufacturer emphasizes the importance of checking the condition of the instrument before any use to detect any visible damage such as cracks or deformations. Due to the materials used, there is no predefined limit of sterilization cycles, but the practitioner's vigilance is required to evaluate wear. Compatibility with other cleaning and disinfection products must also be verified beforehand. Rigorous maintenance is the sine qua non condition for maintaining the performance of the stainless steel and guaranteeing asepsis during endodontic care.
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 applies strict control protocols in accordance with the regulatory requirements applicable to manual dental instruments. Compliance with these standards ensures that the instrument is suitable for professional use in surgical and dental environments. Traceability and compliance with medical stainless steel standards provide practitioners with a reliable tool for their daily interventions in endodontics.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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