Fragment Debrider Heidbrink - Helmut Zepf (17.056.03) - Delynov
The Décortiqueur à Fragments Heidbrink - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.056.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Heidbrink fragment ejector - Helmut Zepf?
The Heidbrink fragment ejector, referenced under code 17.056.03, is a specialized manual instrument designed by Helmut Zepf Medizintechnik GmbH. This device is manufactured from medical-grade stainless steel, ensuring resistance adapted to the mechanical stresses encountered during oral surgery procedures. As a dental fragment extraction instrument, it features a thin and rigid structure allowing access to narrow alveolar areas. This equipment belongs to the category of reusable consumables (CONSO) and is part of a range of instruments intended for practitioners requiring reliable instrumentation for the management of root complications.
What are the clinical indications for this instrument?
This instrument is primarily indicated for the extraction of root fragments and dental debris during exodontia procedures. In oral and implant surgery, the Heidbrink ejector is used when the root fractures below the crestal level, making the use of traditional forceps impossible. It serves to mobilize residual apices by inserting between the alveolar wall and the fragment. Its use is essential for cleaning the socket of all residue before immediate implant placement or to prevent post-operative infectious complications related to the persistence of necrotic or infected dental tissues.
What are the technical characteristics of the 17.056.03 ejector?
The Heidbrink fragment ejector from Helmut Zepf is distinguished by its ergonomic design adapted to the surgeon's hand. Its technical reference 17.056.03 corresponds to a specific model whose working part is optimized for the gripping and luxation of small fragments. Manufactured from medical stainless steel, it offers excellent tactile response when searching for root fragments. Unlike sutures, this instrument does not have a needle but a tapered active tip. It is delivered non-sterile and must imperatively undergo a complete cleaning, disinfection, and sterilization protocol before its first use and after each clinical cycle.
What are the contraindications for the use of this device?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, an allergic reaction may occur in some patients upon contact. If such a hypersensitivity reaction is triggered during the procedure, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, the use of the instrument is strictly prohibited if it shows visible damage such as cracks, breaks, or defects on the cutting edges, in order to avoid any risk of accidental tissue injury.
What are the maintenance and reprocessing precautions?
The Heidbrink ejector is a reusable instrument that requires rigorous reprocessing. Before each use, the practitioner must check for the absence of wear or structural damage. The cleaning and sterilization process must be systematic. Due to the design of the steel and the product, the manufacturer has not defined a maximum limit of treatment cycles, but longevity depends on compliance with decontamination protocols. It is crucial to clean each product before exposing it to the heat of the autoclave to avoid the fixation of organic residues. The use of damaged instruments is dangerous and compromises the safety of the surgical act.
Who is the manufacturer and what standards are respected?
The Heidbrink fragment ejector is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer specifies that all its products must be checked for compatibility with other instruments used during the procedure. Compliance with safety and use instructions is imperative to guarantee conformity with regulatory requirements. This device is exclusively reserved for use by qualified healthcare professionals in dental and oral surgery, thus ensuring an application in accordance with established scientific data.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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