Kocher Hemostatic Forceps 14 cm - Helmut Zepf (23.105.14) - Delynov

What is the Helmut Zepf 14 cm Kocher haemostatic forceps?

The 14 cm Kocher haemostatic forceps, referenced under code 23.105.14 by Helmut Zepf, is a manual instrument designed for surgery. Manufactured from medical stainless steel, this surgical Kocher forceps is distinguished by its robustness and gripping capacity. It belongs to the category of GBR (Guided Bone Regeneration) and general surgery instruments. Its structure is specifically adapted to firmly grasp tissues that are not at risk of tearing, thanks to its serrated jaws. As a Class I medical device, it meets quality requirements for repeated use in a clinical setting, subject to rigorous maintenance.

What are the clinical indications for this instrument?

This haemostatic forceps is primarily indicated in oral, periodontal, and implant surgery for the manipulation of dense tissues. It is used for primary haemostasis by clamping blood vessels, as well as for flap traction or maintaining membranes during reconstruction procedures. Its design allows for solid fixation, preventing slippage during complex surgical maneuvers. It is exclusively reserved for healthcare professionals trained in dental surgical techniques. Its use extends to any procedure requiring significant holding force on non-fragile anatomical structures within the oral cavity.

What are the technical characteristics of the 23.105.14 forceps?

The Helmut Zepf Kocher forceps has a total length of 14 cm, offering an optimal balance between leverage and maneuverability in the restricted space of the oral cavity. It is identified by the technical reference 23.105.14. Manufactured from high-quality medical stainless steel, it is designed to withstand repeated cleaning and sterilization cycles. The instrument is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and must undergo a complete decontamination protocol before its first use and after each intervention. Its mechanical design ensures precise closure and durability in compliance with Class I standards.

What are the contraindications for the use of these forceps?

The main contraindication related to the use of this Helmut Zepf instrument is known hypersensitivity or intolerance to metals, and specifically to medical stainless steel, in the patient. An allergic reaction may occur upon direct contact with tissues. If such a hypersensitivity reaction is triggered during the intervention, the procedure must be stopped immediately and necessary medical measures taken. It is therefore recommended to question the patient about their allergic history before any manipulation. Furthermore, use is prohibited on extremely fragile or friable tissues where the gripping force of the Kocher forceps could cause irreversible damage.

What are the maintenance and reprocessing precautions?

Like any Helmut Zepf surgical instrument, these forceps must be cleaned, disinfected, and sterilized before each use. It is crucial to visually inspect the device for any visible damage or wear, such as cracks, breaks, or defects on the active parts, before proceeding with the surgical act. Never use damaged or worn products. Due to the quality of the materials and design, there is no defined maximum limit of processing cycles, but compatibility with other cleaning products must be verified beforehand. Strict compliance with sterilization protocols guarantees patient safety and instrument longevity.

Who is the manufacturer and what standards are respected?

The forceps are manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. This medical device is classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer requires that all instruments undergo a complete cleaning and sterilization cycle before any use, as they are delivered non-sterile. Compliance with the Helmut Zepf manufacturer instructions is essential to maintain device conformity. The use of this instrument is strictly reserved for qualified healthcare professionals, thus ensuring application in accordance with the rules of the art in dental surgery and appropriate management of risks related to manual instrumentation.

State of the art

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