Dental Fragment Decorticator - Helmut Zepf (17.053.03) - Delynov
The Heidbrink. Décortiqueur à Fragments - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.053.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the Heidbrink Helmut Zepf?
The Heidbrink (reference 17.053.03) is a specialized manual instrument, often referred to as a root fragment elevator. Manufactured by Helmut Zepf Medizintechnik GmbH, this tool is designed from high-quality medical stainless steel to ensure optimal resistance during surgical manipulations. Its thin and rigid structure is specifically adapted to reach narrow areas of the dental socket. This device belongs to the category of reusable consumables, requiring a complete cycle of cleaning, disinfection, and sterilization before each use to maintain hospital hygiene standards.
What are the clinical indications for this fragment elevator?
This instrument is primarily indicated in oral surgery and implantology for the extraction of root fragments or fractured apexes. In clinical practice, the practitioner uses this heidbrink instrument to delicately separate the root fragment from its ligamentous or bony attachments. It can also serve as a fragment syndesmotome to facilitate access during complex extractions where the root is sectioned or deeply anchored. Its use is reserved for qualified healthcare professionals mastering exodontia techniques and the management of root complications.
What are the technical characteristics of instrument 17.053.03?
The Heidbrink Helmut Zepf is distinguished by its ergonomic design favoring a stable grip for high-precision movements. Its working part is sharpened to allow efficient insertion into the periodontal space. Although specific dimensions are not detailed, its technical reference 17.053.03 corresponds to the brand's standards for fragment removal instruments. As a Class I device, it meets the fundamental regulatory requirements for non-invasive or invasive manual surgical instruments for temporary use, guaranteeing compatibility with thermal and chemical reprocessing protocols.
What are the contraindications for the use of this instrument?
The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, specifically medical stainless steel. If an allergic reaction or hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be stopped immediately. Appropriate corrective measures must then be implemented. It is therefore crucial to check the patient's medical history before any surgical intervention involving this metallic instrument to avoid post-operative complications related to an immune reaction.
What are the maintenance and reprocessing precautions?
Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The practitioner must visually inspect the instrument to detect any damage or wear, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited. Due to the robust design of the stainless steel, there is no defined maximum limit for processing cycles, but the longevity of the bone fragment elevator depends on strict compliance with sterilization protocols and careful handling during interventions.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures traceability and production quality in accordance with the requirements for manual dental instruments. Each product, such as the Heidbrink 17.053.03, is subject to rigorous controls to ensure its compliance with safety and performance standards. Healthcare professionals can refer to the safety instructions provided by Helmut Zepf to ensure use in accordance with the intended purposes and clinical indications.
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