Langer periodontal curette, figures 1/2 - Helmut Zepf (24.553.01) - Delynov
The Curette parodontale Langer, figures 1/2 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.553.01.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Langer 1/2 periodontal curette?
The Langer 1/2 periodontal curette, referenced under code 24.553.01 by Helmut Zepf, is a precision manual instrument intended for periodontology. This device combines the design characteristics of a Universal curette with the specific shank of Gracey curettes. It features a rigid structure allowing for optimal force transmission during the removal of calcified deposits. Manufactured by Helmut Zepf Medizintechnik GmbH, this curette is an essential tool for periodontal debridement, offering a double working end to effectively cover the target areas of the mandibular block without multiple instrument changes.
What are the clinical indications for this instrument?
This mandibular periodontal curette is indicated for non-surgical and surgical periodontal debridement. It is primarily used for root planing and deep scaling in the mandible. Its geometry allows access to periodontal pockets to remove subgingival calculus and smooth altered root surfaces. In implant or periodontal surgery, it can be used to clean surgical sites or prepare adjacent tooth surfaces. The use of the Langer 1/2 curette facilitates the treatment of proximal surfaces, thereby contributing to the reduction of gingival inflammation and epithelial reattachment.
What are the technical characteristics of reference 24.553.01?
Technical reference 24.553.01 corresponds to a double-ended active instrument. The Langer 1/2 curette is distinguished by a blade where both edges are sharp, unlike Gracey curettes which only have one. This characteristic allows the practitioner to use the same instrument for the mesial and distal surfaces of the same tooth or the same mandibular quadrant. The shank is angled to provide correct angulation relative to the longitudinal axis of the tooth, ensuring effective contact with the root. Manufacturing by Helmut Zepf guarantees a precise fit of the working parts for consistent cutting efficiency.
What are the contraindications for the use of this curette?
Contraindications for the use of the Langer 1/2 periodontal curette are primarily related to the patient's clinical condition and the nature of the tissues. Its use is discouraged on tooth surfaces presenting severe untreated dentinal hypersensitivity or on fragile prosthetic restorations (veneers, ceramic crowns) that could be scratched by the sharp steel edges. Excessive pressure on very thin alveolar bone or on roots presenting significant external resorptions should also be avoided. As with any manual instrument, a prior assessment of gingival health and bone density is necessary to avoid any iatrogenic trauma.
What are the maintenance and durability precautions?
As a non-resorbable and reusable instrument, the Langer 1/2 curette requires a rigorous sterilization protocol after each use. It is imperative to follow the recommendations of the manufacturer Helmut Zepf regarding cleaning, decontamination, and autoclaving. To maintain the cutting efficiency of the sharp edges, regular sharpening with appropriate sharpening stones is essential. The practitioner must visually inspect the instrument before each procedure to detect any traces of corrosion, micro-cracks, or deformation of the shank. Proper maintenance ensures the longevity of the steel and the safety of the care provided to patients.
Who is the manufacturer and what standards are respected?
The instrument is produced by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of dental and surgical instrumentation. Although the specific regulatory class and CE marking are not detailed in the simplified technical documentation, Helmut Zepf products are designed according to high industrial quality standards specific to reusable medical devices. To obtain precise information on current ISO certifications or compliance with the European Medical Device Regulation (MDR), it is recommended to consult the instructions for use or the declaration of conformity provided by the manufacturer with the instrument.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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