Kelly Haemostatic Forceps curved 14 cm - Helmut Zepf (23.099.14) - Delynov

What is the Helmut Zepf 14 cm curved Kelly hemostatic forceps?

The 14 cm curved Kelly hemostatic forceps is a precision surgical instrument designed by Helmut Zepf Medizintechnik GmbH. This device is characterized by a curved active part and a total length of 14cm, adapted to the constraints of the oral environment. Its articulated structure allows for secure locking to maintain constant pressure on tissues or vessels. It belongs to the category of Guided Bone Regeneration (GBR) instruments distributed by Delynov. Its design aims to offer reliable handling to dental surgeons during critical phases of the intervention, guaranteeing a firm hold without accidental slipping.

What are the clinical indications for this curved Kelly forceps?

In oral surgery and implantology, the curved Kelly forceps is primarily indicated for achieving hemostasis by clamping blood vessels to maintain a clear operative field. It is also used during GBR procedures for grasping and stabilizing membranes, or for handling soft tissue fragments. Its curved shape is particularly relevant for navigating around complex anatomical structures or for reaching the posterior maxillary and mandibular sectors. It also serves as an assistant for passing suture threads or holding auxiliary devices during the surgical act, offering essential versatility in periodontology.

What are the technical characteristics of reference 23.099.14?

Technical reference 23.099.14 corresponds to a specific 14cm model within the Helmut Zepf catalog. This 14cm hemostatic forceps features serrated jaws on their distal part to ensure an atraumatic yet firm grip. The ratchet mechanism allows for adjusting the clamping force according to clinical needs, offering several locking levels. The curvature of the jaws is calculated to optimize the practitioner's visibility while allowing for targeted traction or compression. The instrument's finish is designed to limit reflections under scialytic lighting, thus improving visual comfort during long-duration surgeries.

What are the contraindications for the use of this instrument?

Contraindications related to the use of the Helmut Zepf Kelly forceps are essentially dictated by standard oral surgery protocols. The instrument must not be used for tasks exceeding its mechanical capacities, such as handling dense bone or bending thick titanium plates, which could damage the jaws or the joint. Medically, use is contraindicated in patients with known sensitivities to the metallic components of surgical instrumentation, although these cases are rare. It is the practitioner's responsibility to evaluate the instrument's compatibility with the patient's tissue condition to avoid any excessive trauma during clamping.

What are the maintenance precautions for this Helmut Zepf forceps?

Like any non-resorbable surgical instrument, the 14cm Kelly forceps requires a rigorous sterilization and maintenance protocol after each use. It is imperative to follow the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH regarding manual or ultrasonic cleaning, as well as autoclave cycles. Particular attention must be paid to the joint and the ratchet to prevent the accumulation of biological residues or scale deposits that could seize the mechanism. Complete drying is necessary before sterilization to prevent any risk of corrosion. Regular checking of the jaw alignment guarantees the long-term performance of the instrument's grip.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-quality dental and surgical instrumentation. Although detailed regulatory specifications such as the exact class or specific CE marking are not mentioned in the current source data, Helmut Zepf products are developed according to strict manufacturing standards to meet the requirements of healthcare professionals. For any precise information regarding certificates of conformity or ISO standards applied to reference 23.099.14, it is recommended to consult the instructions for use or contact Delynov's technical service directly.

State of the art

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