Desmotome for Separation - Helmut Zepf (26.183.00) - Delynov
The Desmotome pour la séparation - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 26.183.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf desmotome for separation?
The desmotome for separation, referenced under code 26.183.00, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. Manufactured from high-quality medical stainless steel, this device is specifically structured to intervene on the soft tissues surrounding the tooth. As a syndesmotome, its primary role is to allow the practitioner to access the periodontal space. Its rigid and thin design ensures handling adapted to the requirements of oral surgery. This product belongs to regulatory Class I, guaranteeing its compliance with basic standards for non-invasive or invasive instruments for temporary use.
What are the clinical indications?
This instrument is indicated for all dental surgery procedures requiring a clean separation of periodontal tissues. Its primary use lies in syndesmotomy, an indispensable preliminary step to dental extraction to break the ligament fibers that hold the tooth in its socket. By separating the epithelial attachment and the connective fibers, the Helmut Zepf desmotome facilitates the subsequent insertion of forceps or elevators, thereby limiting the stress exerted on the surrounding alveolar bone. It is exclusively reserved for use by healthcare professionals qualified in the context of oral care.
What are the technical characteristics?
The Helmut Zepf desmotome (26.183.00) is distinguished by its medical stainless steel composition, a material chosen for its resistance and its ability to withstand decontamination cycles. Although delivered non-sterile, the instrument is designed to undergo complete reprocessing including cleaning, disinfection, and sterilization. The manufacturer Helmut Zepf Medizintechnik GmbH specifies that, given the design of the product and the materials used, there is no defined maximum limit for the number of processing cycles achievable. Its ergonomic structure allows for precise force transmission during tissue separation without compromising the integrity of the instrument.
What are the contraindications for use?
The main medical contraindication related to the use of this desmotome is the patient's known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, direct contact can trigger an allergic reaction in sensitive subjects. The manufacturer warns that if such a hypersensitivity reaction occurs during the procedure, the procedure must be stopped immediately and the necessary medical measures must be taken accordingly. It is therefore imperative to check the patient's allergic history before any manipulation with this manual instrument.
What are the maintenance and safety precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. A visual inspection is crucial before each intervention to detect any possible damage or visible wear, such as cracks, breaks, or defects on the cutting edges. It is strictly forbidden to use damaged or worn products, as this could compromise patient safety and the effectiveness of the surgical procedure. Compatibility with other products used during the operative act must also be verified beforehand by the healthcare professional.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with the regulatory requirements for Class I medical devices. Although the specific CE marking is not detailed in the technical data provided, the instrument complies with manufacturing standards for medical stainless steel intended for surgical use. As a Class I product, it meets the safety and performance protocols defined for manual dental instruments. The reprocessing and maintenance of the instrument are the responsibility of the healthcare professional, in accordance with the instructions provided by Helmut Zepf.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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