Micro serrated anatomical forceps - Helmut Zepf (22.820.17TC) - Delynov

What is the Helmut Zepf micro anatomical forceps?

The micro anatomical forceps (reference 22.820.17TC) is a precision instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed from high-quality medical stainless steel, it is distinguished by its serrated jaws which optimize grip without compromising the integrity of soft tissues. This device is specifically developed to meet the requirements of micro-surgery and guided bone regeneration (GBR). Its fine structure allows for easy manipulation in restricted access areas, offering practitioners a reliable tool for delicate interventions requiring high dexterity.

What are the clinical indications for these serrated jaw surgical forceps?

These serrated jaw surgical forceps are primarily indicated for the atraumatic holding and grasping of tissues during various oral surgical interventions. They are used to stabilize flaps, handle membranes in implant surgery, or grasp soft tissues during biopsies. Beyond tissue manipulation, they are perfectly suited for holding or removing foreign bodies, managing sutures during knotting, or handling swabs in the operative field. Their use is strictly reserved for qualified healthcare professionals mastering oral surgery protocols.

What are the technical characteristics of the 22.820.17TC forceps?

The Helmut Zepf serrated jaw anatomical forceps, referenced under code 22.820.17TC, are manufactured from medical stainless steel, guaranteeing resistance to repeated sterilization processes. Its micro anatomical design is optimized for maximum ergonomics during fine gripping phases. The serrated jaws are developed to provide sufficient friction to hold tissues or suture threads without slipping, while limiting mechanical trauma. As a Class I instrument, it meets the rigorous manufacturing requirements of the manufacturer Helmut Zepf Medizintechnik GmbH for durable use in dental practices.

What are the contraindications for the use of this instrument?

The main contraindication related to the use of these micro anatomical forceps concerns patients with a known hypersensitivity or intolerance to metals, particularly medical stainless steel. Contact of the instrument with tissues can trigger a hypersensitivity reaction in these subjects. The manufacturer specifies that the surgical procedure must be immediately stopped if such an allergic reaction occurs, and necessary clinical measures must be taken accordingly. It is therefore recommended to check the patient's allergic history before any intervention.

What are the maintenance and sterilization precautions?

Like any non-sterile surgical instrument from the Helmut Zepf brand, these forceps must imperatively be cleaned, disinfected, and sterilized before their first use, as well as after each subsequent use. The reprocessing process must be complete to guarantee patient safety. Before each use, the practitioner must inspect the instrument to detect any visible damage such as cracks, breaks, or defects on the active parts. It is formally discouraged to use a damaged or worn product. Due to its robust design, there is no defined maximum limit of treatment cycles, as long as functional integrity is preserved.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer in the field of dental instrumentation ensures production compliant with European quality standards. The product is classified as a Class I medical device according to current regulations. It is delivered non-sterile and requires a rigorous sterilization protocol before any clinical application. Traceability is ensured by the technical reference 22.820.17TC, allowing practices to maintain precise monitoring of their surgical instrument fleet.

State of the art

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