Dissecting Forceps with Claws - Helmut Zepf (22.812.17) - Delynov.
The Pince à dissection à griffes - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.812.17.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf clawed dissection forceps?
The clawed dissection forceps, referenced under code 22.812.17 by Helmut Zepf, is a manual instrument specifically developed for oral surgery. Manufactured from high-quality medical stainless steel, this forceps is distinguished by its clawed tip, designed to provide a firm grip on tissues. Its structure allows for precise manipulation during delicate tissue separation phases. As an instrument in the GBR (Guided Bone Regeneration) category, it meets the durability and resistance requirements necessary for sterile clinical environments. This device is delivered non-sterile and requires a rigorous preparation protocol before any intervention.
What are the clinical indications for this instrument?
This manual dental instrument is primarily indicated for the manipulation of soft tissues during invasive surgeries. In implantology and periodontology, the dissection forceps is used to lift, hold, or retract epithelial-connective tissue flaps. The claws allow for tissue stabilization without requiring excessive pressure that could compromise local vascularization. It is particularly useful during guided bone regeneration (GBR) procedures where precise tissue positioning is crucial for graft success. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.
What are the technical characteristics of reference 22.812.17?
Technical reference 22.812.17 corresponds to a clawed dissection forceps from the Helmut Zepf brand. It is forged from medical stainless steel selected for its biocompatibility and corrosion resistance. Its ergonomic design allows for optimal tactile control, essential during meticulous dissections. Unlike smooth-jawed forceps, the claws of this model ensure superior mechanical retention on dense or fibrous tissues. The instrument is designed to withstand repeated cycles of cleaning, disinfection, and sterilization, although no maximum cycle limit is defined by the manufacturer Helmut Medizintechnik GmbH due to the robustness of the materials used.
What are the contraindications for using this forceps?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known patient hypersensitivity to metals. As the instrument is composed of medical stainless steel, direct contact may trigger an intolerance or hypersensitivity reaction in certain individuals. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Additionally, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the effectiveness of the surgical maneuver.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the very first use, as well as after each subsequent use. The reprocessing process must be complete to guarantee asepsis. It is crucial to visually inspect the forceps before each intervention to detect any signs of wear or damage. Never use a damaged product. As the devices are delivered non-sterile, compliance with autoclave sterilization protocols is mandatory. The manufacturer specifies that the number of achievable treatment cycles depends on the design and maintenance, with no fixed limit being imposed as long as the functional integrity of the steel is preserved.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to current regulations. The manufacturer ensures the conformity of its production processes to meet the requirements of healthcare professionals. As a Class I instrument, it complies with the safety and performance standards applicable to reusable manual dental instruments. The traceability and manufacturing quality of the Helmut Zepf brand guarantee a reliable tool for daily oral surgery interventions in dental offices or hospital settings.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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