Hartmann Hemostatic Forceps - Helmut Zepf (23.050.10) - Delynov

What is the Hartmann hemostatic forceps - Helmut Zepf (23.050.10)?

The Hartmann hemostatic forceps, referenced under code 23.050.10, is a manual surgical instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device is made of medical-grade stainless steel, guaranteeing resistance adapted to the constraints of oral surgery. Its structure is specifically designed to offer a fine and precise grip, typical of instruments in the Helmut Zepf range. As an instrument in the GBR (Guided Bone Regeneration) category, it is integrated into surgical protocols requiring rigorous manipulation of tissues and small vessels.

What are the clinical indications for these surgical hemostatic forceps?

These surgical hartmann forceps are primarily indicated for performing primary hemostasis during oral, implant, or periodontal surgery interventions. They allow the practitioner to effectively clamp small blood vessels in order to maintain optimal visibility of the surgical site. Beyond its hemostasis function, it is used for the manipulation of soft tissues, holding membranes, or assistance during complex sutures. Its use is strictly reserved for qualified healthcare professionals operating in sterile clinical environments for manual dental surgery procedures.

What are the technical characteristics of the Hartmann forceps (23.050.10)?

The Hartmann Helmut Zepf forceps are distinguished by their medical stainless steel design, a material chosen for its biocompatibility and its ability to undergo repeated sterilization cycles. Although delivered non-sterile, they are designed to withstand the cleaning, disinfection, and sterilization processes required before each use. Their compact geometry, specific to the Hartmann model, facilitates access to restricted areas of the oral cavity. Reference 23.050.10 corresponds to a precision standard at Helmut Zepf Medizintechnik GmbH, ensuring stable closure and reliable locking during tissue or vessel clamping.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or metal intolerance in the patient. Since the instrument is composed of medical stainless steel, direct contact can trigger an allergic reaction in sensitive subjects. If such a reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore imperative to check the patient's history regarding allergies to metallic components before any use of these hemostatic forceps in the mouth.

What are the maintenance and reprocessing precautions for this device?

Like any Helmut Zepf instrument, these forceps must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The practitioner must perform a thorough visual inspection to detect potential damage such as cracks, breaks, or defects on the active parts. The use of a damaged or worn instrument is strictly prohibited. Due to its robust design and the materials used, there is no defined maximum limit of processing cycles, but the longevity of the device depends directly on compliance with cleaning protocols and the absence of visible wear noted by the professional.

Who is the manufacturer and what standards are respected?

The Hartmann hemostatic forceps are manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer specifies that the products are delivered non-sterile and must undergo complete reprocessing by the end user. Compliance with the safety and use instructions provided by Helmut Zepf is essential to guarantee patient safety and instrument performance. Compatibility with other surgical devices used simultaneously must also be verified by the practitioner before the intervention.

State of the art

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