Proximal Desmotome Tissue Dissector - Helmut Zepf (17.418.00) - Delynov
The Désignateur de tissu desmotome proximal - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.418.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf proximal desmotome tissue designator?
The proximal desmotome tissue designator, referenced under code 17.418.00, is a manual surgical instrument developed by the manufacturer Helmut Zepf Medizintechnik GmbH. Constructed from medical stainless steel, this device belongs to the category of Class I consumables and instruments. Its structure is specifically designed for intervention in narrow proximal spaces, offering rigorous handling during the initial phases of oral surgery. As a non-sterile instrument upon delivery, it requires a complete cleaning, disinfection, and sterilization protocol before each use to ensure clinical safety.
What are the clinical indications for this instrument?
The Helmut Zepf proximal desmotome is indicated for sectioning the periodontal ligaments (desmodontium) prior to extraction or during periodontal surgery procedures. Its use is particularly relevant for preserving the integrity of the alveolar bone and marginal gingiva by limiting trauma during avulsion. In implant surgery, it assists in site preparation by allowing clean separation of soft tissues. This device is exclusively reserved for healthcare professionals trained in dental and oral surgery techniques, ensuring application in accordance with good clinical practices.
What are the technical characteristics of the 17.418.00 desmotome?
This Class I medical device is distinguished by its manufacture from high-quality medical stainless steel, selected by Helmut Zepf for its resistance and ability to withstand repeated reprocessing cycles. Reference code 17.418.00 designates a specific proximal configuration, adapted to the anatomy of interdental areas. Although the manufacturer does not define a maximum limit for sterilization cycles, the instrument must undergo rigorous visual inspection before each use. Any sign of damage, such as cracks, breaks, or wear of the cutting edges, requires the immediate removal of the product from the clinical circuit.
What are the contraindications for the use of this device?
The main contraindication related to the use of the Helmut Zepf tissue designator lies in the patient's known hypersensitivity or intolerance to metals, particularly components of medical stainless steel. An allergic reaction may be triggered upon direct contact with the instrument. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and appropriate medical measures must be initiated. It is the practitioner's responsibility to verify the patient's allergic history before any surgical manipulation with this manual instrument.
What are the maintenance and sterilization precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as between each patient. The reprocessing process must be complete and follow standard sterilization protocols in force in dental practices. It is crucial to carefully clean each product to remove any organic residue before autoclaving. The practitioner must also verify compatibility with other instruments used simultaneously. The use of damaged products or those with visible defects on the active parts is strictly prohibited.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer complies with the safety and performance requirements applicable to manual dental instruments. As a recognized supplier in the field of precision instrumentation, Helmut Zepf guarantees the use of materials compliant with medical standards, such as stainless steel. Traceability is ensured by technical reference 17.418.00, allowing healthcare professionals to verify the origin and compliance of the equipment used in their operating room.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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