Hemostatic Forceps Kelly - Helmut Zepf (23.098.14) - Delynov

What is the Helmut Zepf (23.098.14) Kelly forceps?

The Helmut Zepf Kelly forceps, referenced under code 23.098.14, is a manual instrument specifically designed for oral surgery environments. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this surgery kelly forceps is distinguished by its robust structure and its ability to maintain constant pressure on tissues or vessels. It belongs to the category of GBR (Guided Bone Regeneration) instruments and meets the quality requirements for Class I devices. Its design allows for easy handling by the practitioner during critical phases of the intervention.

What are the clinical indications for this kelly forceps?

In clinical practice, the dental kelly forceps is primarily indicated for hemostasis. It is used to clamp blood vessels to interrupt blood flow or to firmly grasp soft tissues during periodontal or implant surgeries. Its configuration as a curved hemostatic forceps makes it particularly useful for accessing restricted anatomical areas in the oral cavity, thus facilitating the surgeon's work during flap procedures or complex extractions. It also serves for handling small sterile elements during the operative protocol.

What are the technical characteristics of this instrument?

This Helmut Zepf Kelly forceps features technical characteristics adapted to the constraints of modern dental surgery. Identified by reference 23.098.14, it is manufactured from a medical stainless steel selected for its resistance to processing cycles. As a Class I instrument, it is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH. Its curved shape is optimized to offer maximum visibility to the practitioner while guaranteeing a secure grip. The product design does not define a maximum limit of processing cycles, although wear must be checked before each use.

What are the contraindications for the use of the Kelly forceps?

The main contraindication related to the use of this surgery kelly forceps concerns known hypersensitivity of patients to metals. As the instrument is composed of medical stainless steel, contact may trigger an allergic reaction in intolerant subjects. If such a reaction occurs during the intervention, the manufacturer Helmut Zepf stipulates that the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any use of this manual instrument in the mouth.

What are the maintenance and reprocessing precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and must imperatively follow a complete cleaning, disinfection, and sterilization protocol before the first use and after each subsequent use. It is essential to visually inspect the curved hemostatic forceps to detect any 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 design and the materials used, there is no predefined limit of reprocessing cycles, but compatibility with other products must be verified beforehand.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as a Class I instrument according to current regulations. The manufacturer insists that the use of this kelly forceps is reserved exclusively for qualified healthcare professionals. Compliance with safety instructions, notably systematic cleaning and sterilization, is mandatory to guarantee patient safety and the longevity of the instrument. Helmut Zepf is recognized for the quality of its medical devices intended for dental surgery.

State of the art

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