Hemostatic Forceps Kocher 14 cm - Helmut Zepf (23.104.14) - Delynov

What is the Kocher 14 cm Helmut Zepf hemostatic forceps?

The Kocher 14 cm hemostatic forceps is a manual surgical instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. Used primarily in oral surgery, these forceps are distinguished by their robust medical stainless steel structure. It belongs to the category of GBR (Guided Bone Regeneration) and periodontology instruments. Its specific configuration, including serrated jaws, allows for a firm grip on tissues. This device is referenced under code 23.104.14 and is part of the range of high-precision instruments intended for dental operating theaters.

What are the clinical indications for these dental Kocher forceps?

The dental Kocher forceps are indicated for various oral and implant surgery maneuvers. Its primary role is to ensure hemostasis by compressing vessels, but it is also used for handling resistant tissues, flaps, or suture material during critical phases of the procedure. In reconstructive surgery, it facilitates the holding of membranes or the stabilization of soft tissues. Its length of 14 cm provides leverage and visibility suitable for both posterior and anterior areas of the oral cavity, ensuring precise handling for dental surgeons and implantologists.

What are the technical characteristics of the 14 cm Kocher forceps?

The 14 cm Kocher forceps (reference 23.104.14) feature rigorous technical specifications adapted to medical requirements. Manufactured in medical stainless steel by Helmut Zepf, it has a total length of 14 cm, giving it optimal maneuverability in confined environments. This device is classified as a Class I instrument according to medical device regulations. It is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before each use. Its design allows it to withstand repeated processing cycles, although a visual inspection to detect any cracks or wear is imperative before any procedure.

What are the contraindications for using this instrument?

The use of this instrument is contraindicated in patients with a known intolerance or hypersensitivity to metals, specifically medical stainless steel. Contact with the instrument could trigger an allergic reaction. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that the intervention must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of products with visible damage, such as cracks, breaks, or defects on the cutting edges, is strictly prohibited to ensure patient safety.

What are the maintenance and reprocessing precautions?

Like any non-sterile Class I instrument, the Kocher hemostatic forceps must imperatively be cleaned, disinfected, and sterilized before its first use and after each subsequent use. The manufacturer emphasizes the importance of thorough cleaning to remove any residue before the sterilization cycle. Due to its design and the materials used, there is no defined maximum limit for processing cycles, as long as the instrument shows no functional wear or structural damage. It is reserved exclusively for trained healthcare professionals, who must verify compatibility with other products used simultaneously.

Who is the manufacturer and what standards are met?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is a Class I instrument, compliant with regulatory requirements relating to medical devices (MDR). Traceability is ensured by technical reference 23.104.14. As a manual stainless steel instrument, it meets hospital-grade quality standards for dental surgery. Compliance with the reprocessing protocols described by Helmut Zepf is essential to maintain the conformity and safety of the instrument during its use in offices or clinics.

State of the art

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