Miller-Colburn surgical file for osteotomy and alveolotomy, fig. 2 - Helmut Zepf (41.881.12) - Delynov
The Flèche chirurgicale pour ostéotomie et alvéolotomie Miller-Colburn, figure 2 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.881.12.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Miller-Colburn figure 2 surgical bone file?
The Miller-Colburn surgical bone file, figure 2, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This device is specifically designed for bone surgery interventions within the oral cavity. Its structure is optimized for cutting and separating hard tissues, offering a response adapted to the needs of dental surgeons and implantologists. As an instrument in the Helmut Zepf range, it benefits from the technical expertise of this recognized manufacturer in the field of high-quality medical instrumentation for osteotomy and alveolotomy.
What are the clinical indications for this instrument?
The use of the Miller-Colburn figure 2 bone file is primarily indicated in two types of oral surgical procedures: osteotomy and alveolotomy. In clinical practice, it is used to section, remodel, or remove bone segments, particularly during the preparation of an implant site or during alveoloplasty after a tooth extraction. This instrument allows for the treatment of alveolar bone structures with the precision required to promote optimal tissue healing. Its design is particularly useful for accessing areas requiring targeted intervention on the maxillary or mandibular bone.
What are the technical characteristics of reference 41.881.12?
Reference 41.881.12 corresponds to the specific Miller-Colburn figure 2 model from the Helmut Zepf catalog. This instrument is distinguished by its arrow shape, a geometry designed to facilitate the surgical movement during bone penetration or separation. Although specific material details are not listed in the source data, the manufacturing standards of Helmut Zepf Medizintechnik GmbH guarantee an instrument suitable for the constraints of sterilization and repeated use in a surgical environment. Its ergonomic design ensures a stable grip for rigorous control during alveolotomy.
What are the contraindications for the use of this instrument?
Contraindications for the use of the Miller-Colburn figure 2 surgical bone file are related to the general limits of oral bone surgery. It should not be used if the bone volume is insufficient to support the intervention or if the patient presents with serious systemic pathologies contraindicating invasive surgery. Additionally, the use of this instrument is prohibited in cases of known allergy to the metallic components of standard surgical instrumentation. It is the practitioner's responsibility to evaluate the benefit-risk ratio based on the patient's general health status and the complexity of the planned osteotomy.
What are the precautions for use and maintenance?
As a non-resorbable and reusable surgical instrument, the Miller-Colburn bone file requires a rigorous decontamination and sterilization protocol after each use, in accordance with the directives from the manufacturer Helmut Zepf. It is imperative to check the integrity of the working part before each intervention to ensure the absence of deformation or premature wear that could compromise the precision of the alveolotomy. Storage must be carried out in a dry and clean environment to preserve the mechanical properties of the steel and guarantee the longevity of the device within the dental practice.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, an internationally renowned German company specializing in dental and surgical instrumentation. Although the specific regulatory class and CE marking are not explicitly detailed in the available source data, Helmut Zepf is recognized for respecting the high quality standards specific to European medical devices. For any precise information regarding regulatory certifications or ISO standards applied to reference 41.881.12, it is recommended to refer to the instructions for use or the technical documentation provided by the manufacturer.
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Specifications
| Manufacturer | Helmut Zepf |
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