Elevator X - DESMO - TOOL - Helmut Zepf (17.007.05) - Delynov,
The Élévateur X - DESMO - Instrument - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.007.05.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf X - DESMO elevator?
The X - DESMO elevator (reference 17.007.05) is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in high-quality medical stainless steel, this instrument is specifically dedicated to extraction surgery. Its structure is designed to meet the needs of dental surgeons when handling hard and soft tissues surrounding the tooth. As a syndesmotome desmo type instrument, it is used to initiate the luxation movement. This device belongs to Class I of medical devices, guaranteeing its compliance with regulatory requirements for non-invasive or invasive instruments for temporary use.
What are the clinical indications for this instrument?
The main indication for this Helmut Zepf instrument is the elevation of teeth or residual dental roots during an extraction. In clinical practice, it serves as a desmotome luxator to break the ligament attachments (periodontal ligament) before using forceps. It is particularly useful for mobilizing fractured roots or those deeply anchored in the socket. Its use occurs in the initial phases of avulsion to minimize mechanical resistance. The practitioner uses it to create space between the root and the alveolar wall, thus facilitating a smoother extraction of residual dental elements.
What are the technical characteristics of instrument 17.007.05?
Instrument 17.007.05 is characterized by a straight design, often identified under the name XTool 5 straight 4.0mm in the surgical sector. Manufactured in medical stainless steel, it exhibits the high resistance necessary for the leverage forces applied during syndesmotomy. Its working part is optimized to insert precisely into the periodontal space. This instrument is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and requires a complete processing protocol before its first use. Its robust design allows for repeated reprocessing in an autoclave, although a visual inspection of the cutting edges is imperative before each procedure to detect any possible cracks or breaks.
What are the contraindications for the use of this elevator?
The main medical contraindication related to the use of this instrument is known hypersensitivity or intolerance of the patient to metals, specifically to medical stainless steel. A hypersensitivity reaction can be triggered upon contact with the instrument. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf specifies that the procedure must be immediately stopped and that the necessary medical measures must be taken accordingly. It is therefore recommended to evaluate the patient's allergic history before any surgical manipulation with metal instruments.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The cleaning process must be complete to eliminate all organic residue. Before sterilization, the practitioner must perform a visual check to identify damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited. Due to the quality of the materials used, there is no defined maximum limit of sterilization cycles, but functional wear must remain the primary criterion for retiring the instrument.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as Class I according to the Medical Device Regulation (MDR). The manufacturer ensures the compliance of its products with current safety and performance standards for manual dental instruments. Traceability is ensured by the reference code 17.007.05. As a Class I medical device, it meets the rigorous manufacturing requirements for medical stainless steel, thus guaranteeing safe use in a professional surgical environment by qualified healthcare practitioners.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |