Micro dissecting forceps with claws - Helmut Zepf (22.810.17D) - Delynov

What is the Helmut Zepf 22.810.17D micro-dissection forceps?

The micro-dissection tissue forceps with teeth, referenced under code 22.810.17D by Helmut Zepf, is a precision instrument manufactured from high-quality medical stainless steel. This surgical micro-forceps is specifically designed for procedures requiring high manipulation finesse in the oral cavity. Its lightweight structure and toothed tips allow for a firm yet controlled grip of soft tissues or auxiliary materials. As a Class I device, it meets the safety requirements for non-invasive or short-term invasive reusable surgical instruments. Its robust design ensures durability suitable for the repetitive sterilization cycles required in a clinical environment.

What are the clinical indications for these dissection forceps?

These dissection forceps are indicated for a wide range of applications in oral and implant surgery. Its intended purpose is to allow the practitioner to hold or grasp tissues in a surgical or atraumatic manner during the operative act. It is also particularly useful for manipulating small objects such as foreign bodies present in the site, suture threads during flap closure, or swabs for hemostasis. Its precision makes it a tool of choice for guided bone regeneration (GBR) procedures where the delicate manipulation of membranes and gingival tissues is crucial to the success of the intervention.

What are the technical characteristics of this instrument?

The Helmut Zepf 22.810.17D instrument is distinguished by its medical stainless steel construction, a material selected for its corrosion resistance and compatibility with thermal cleaning processes. Although specific dimensions are not listed, its 'micro-forceps' designation indicates a tip fineness adapted to restricted spaces. The device is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. The manufacturer states that due to the design and materials used, there is no defined maximum limit for the number of processing cycles, subject to proper maintenance.

What are the contraindications for using these micro-forceps?

The main contraindication related to the use of these micro-dissection forceps is the patient's known hypersensitivity to metals, particularly medical stainless steel. Contact with the instrument could trigger a hypersensitivity reaction in intolerant subjects. The manufacturer, Helmut Zepf Medizintechnik GmbH, stipulates that the surgical procedure must be immediately interrupted if such a reaction occurs, and that necessary medical measures must be taken accordingly. It is therefore recommended to check the patient's allergic history before any intervention using metallic instruments.

What are the maintenance and safety precautions?

To ensure patient safety and instrument longevity, all Helmut Zepf devices must be cleaned, disinfected, and sterilized before the first use and after each use. It is imperative to visually inspect the product before each intervention to detect any potential damage or visible wear, such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn instrument is strictly prohibited. Additionally, compatibility with other products used simultaneously must be verified beforehand. Reprocessing must follow standard hospital sterilization protocols to maintain the integrity of the stainless steel.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. As a recognized manufacturer in the surgical instrumentation sector, Helmut Zepf guarantees products that comply with quality requirements for professional use by qualified healthcare providers. The products are delivered non-sterile and their maintenance is the responsibility of the professional, in accordance with the instructions provided by Helmut Zepf Medizintechnik GmbH to ensure safe and effective use in surgery.

State of the art

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