Modified surgical dental extraction forceps according to Dr. Beck, English pattern 17 cm, stainless steel - Helmut Zepf (12.217.00Z) - Delynov
The Davier chirurgical modifié selon Dr. Beck, forme anglaise 17 cm, acier inoxydable - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 12.217.00Z.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the modified surgical extraction forceps according to Dr. Beck?
The modified surgical extraction forceps according to Dr. Beck, referenced under code 12.217.00Z by Helmut Zepf, is a manual instrument used for dental extraction. This model adopts a specific English pattern with a total length of 17 cm. It is manufactured in stainless steel, a preferred material in clinical settings for its corrosion resistance and its ability to withstand repeated sterilization cycles. This stainless steel forceps is distinguished by its modified configuration which optimizes grip and the application of forces during luxations and the extractions themselves.
What are the clinical indications for this instrument?
This Beck forceps is primarily indicated for exodontia procedures in oral surgery and implantology. Its use is intended for the firm grasping of the dental organ or root fragments in order to perform a complete avulsion. Thanks to its modified ergonomic design, it allows the practitioner to exercise the rotation or tilting movements necessary to break the periodontal ligament fibers. It is suitable for both scheduled interventions and emergency extractions, adapting to the requirements of dental surgeons and stomatologists.
What are the technical characteristics of this forceps?
The surgical forceps produced by Helmut Zepf presents precise technical specifications to meet dental surgery standards. It measures exactly 17 cm, offering an adequate lever arm for extractions requiring controlled force. Its stainless steel manufacturing guarantees increased longevity and irreproachable hygiene. The technical reference 12.217.00Z corresponds to the English pattern variant modified by Dr. Beck, characterized by a specific beak geometry allowing for optimal adaptation to the targeted dental anatomy.
What are the contraindications for the use of this forceps?
The contraindications for using this stainless steel surgical forceps are essentially related to the patient's clinical state and the nature of the tooth to be extracted. It must not be used if the morphology of the tooth does not correspond to the shape of the instrument's beaks, at the risk of causing an unwanted crown or root fracture. Furthermore, as with any stainless steel instrument, a known hypersensitivity of the patient to the alloy components (such as nickel or chromium) must be taken into account by the practitioner before any intervention.
What are the maintenance precautions for this non-absorbable instrument?
As a reusable metallic instrument and not an absorbable device, the Helmut Zepf forceps requires a rigorous decontamination and sterilization protocol after each use. It is imperative to follow the manufacturer's recommendations regarding manual or ultrasonic cleaning, as well as autoclave parameters. Complete drying is necessary to prevent any trace of oxidation. The practitioner must regularly inspect the joint and the condition of the beaks to ensure the absence of wear or deformation that could compromise the safety of the surgical act.
Who is the manufacturer and what standards are respected?
This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-precision dental instrumentation. Although specific details of the regulatory class or CE marking are not mentioned in the current technical sheet, Helmut Zepf products are designed according to rigorous industrial quality standards specific to reusable medical devices. To obtain precise information on compliance certifications or to consult the instructions for use, it is recommended to refer to the official documents provided by the manufacturer with the instrument.
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