Micro-dissection forceps with claws - Helmut Zepf (22.811.17) - Delynov

What is the Helmut Zepf micro tissue forceps with teeth (22.811.17)?

The micro tissue forceps with teeth, referenced under code 22.811.17 by the manufacturer Helmut Zepf Medizintechnik GmbH, is a precision instrument intended for oral surgery. Manufactured from medical stainless steel, this surgical micro forceps is specifically designed to offer a stable grip thanks to its toothed tip. It belongs to the Class I instrument category, ensuring its compliance with regulatory requirements for non-invasive or reusable surgical instrumentation after processing. Its fine structure allows intervention in areas of restricted access, facilitating the practitioner's work during delicate phases of dissection or tissue manipulation.

What are the clinical indications for this surgical micro forceps?

This Helmut Zepf micro tissue forceps with teeth is indicated for surgical holding and grasping of tissues during invasive procedures. Its main application is in implantology and periodontology, particularly during guided bone regeneration (GBR) protocols. Beyond tissue manipulation, it is officially intended for holding or removing foreign bodies, and manipulating sutures or swabs during surgery. Its use is strictly reserved for qualified healthcare professionals, ensuring handling adapted to the requirements of dental and oral micro-surgery.

What are the technical characteristics of this instrument?

The Helmut Zepf micro forceps (ref. 22.811.17) is distinguished by its high-quality medical stainless steel design. Although delivered non-sterile, it is designed to withstand repeated cycles of cleaning, disinfection, and sterilization without a defined maximum limit of cycles, provided there is no visible damage. The instrument features teeth at its tip to ensure effective prehension. As a Class I device, it meets the manufacturing standards of Helmut Zepf Medizintechnik GmbH. Before each use, it is imperative to check for the absence of cracks, breaks, or defects on the active parts to ensure operative safety.

What are the contraindications for the use of the micro forceps with teeth?

The main contraindication related to the use of this Helmut Zepf instrument is the patient's known hypersensitivity or intolerance to metals, particularly medical stainless steel. A hypersensitivity reaction can be triggered upon contact between the instrument and the tissues. If such a reaction occurs during the procedure, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to validate the absence of metal allergies during the preoperative anamnesis. Furthermore, the use of an instrument showing signs of wear, corrosion, or structural damage is formally prohibited.

What are the maintenance and reprocessing precautions?

Helmut Zepf brand products are delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, and then after each subsequent use. Reprocessing must follow standard surgical environment protocols. Due to the materials used, there is no predefined limit for treatment cycles, but the longevity of the micro forceps with teeth depends on systematic inspection by the practitioner. Any instrument showing cracks, defective cutting edges, or signs of breakage must be removed from service to avoid any risk of intraoperative complications.

Who is the manufacturer and what standards are respected by this device?

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 traceability and quality of the medical stainless steel used for the design of this micro tissue forceps. Compliance with the safety and use instructions provided by Helmut Zepf is essential to maintain the device's conformity during its integration into the surgical workflow. The instrument is specifically dedicated to professional use by experts in the dental and medical sector.

State of the art

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