Micro Dissection Forceps - Helmut Zepf (22.820.17D) - Delynov

What is the Helmut Zepf micro dissection forceps?

The Helmut Zepf micro dissection forceps, referenced under code 22.820.17D, is a precision instrument intended for oral surgery. Manufactured from high-quality medical stainless steel, these precision surgical forceps are specifically designed for the delicate manipulation of soft tissues and auxiliary materials in a clinical setting. As a Class I device, it meets the safety requirements for temporary-use invasive instruments. Its fine structure allows for a stable grip while minimizing tissue trauma, which is essential for micro-surgery and periodontology protocols.

What are the clinical indications for this instrument?

This instrument is indicated for the atraumatic holding or grasping of tissues during surgical procedures. In the context of implant surgery or GBR (Guided Bone Regeneration), it allows for precise flap manipulation. It is also used to hold or remove foreign bodies, manipulate sutures during wound closure, or manage swabs during the operative act. Its use is strictly reserved for qualified healthcare professionals, ensuring application in accordance with current clinical standards.

What are the technical characteristics of the 22.820.17D forceps?

The Helmut Zepf dental micro dissection forceps is distinguished by its medical stainless steel construction, a material chosen for its strength and biological compatibility. This 22.820.17D model is designed to provide optimal tactile response to the practitioner. Delivered non-sterile, it requires a complete cycle of cleaning, disinfection, and sterilization before each use. The manufacturer does not define a maximum limit for processing cycles, as longevity depends on maintenance and the absence of visible damage such as cracks or defects on the edges.

What are the contraindications for the use of these forceps?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns metal intolerance. A hypersensitivity reaction may be triggered in certain patients upon contact with medical stainless steel. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any use of this metallic instrument in the mouth.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to visually inspect the product to detect potential damage or wear, such as cracks, breaks, or defects on the active parts. Never use damaged or worn products. Furthermore, compatibility with other surgical devices used simultaneously must be verified beforehand to ensure patient safety and the integrity of the instrumentation.

Who is the manufacturer and what standards are respected?

The micro forceps is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer emphasizes that its products are delivered non-sterile and must undergo rigorous reprocessing by healthcare professionals. The design of the instrument and the materials used allow for durable reuse, subject to strict compliance with the cleaning and sterilization protocols recommended by the manufacturer.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.