Micro Preccelle D'APRES COOLEY - Helmut Zepf (22.815.17) - Delynov (Dental Surgery Products)

What is the micro forceps ACCORDING TO COOLEY Helmut Zepf?

The micro forceps ACCORDING TO COOLEY, referenced under code 22.815.17 by the manufacturer Helmut Zepf Medizintechnik GmbH, is a precision instrument intended for micro-surgery. Manufactured from medical stainless steel, this dental cooley forceps is specifically structured to offer a stable grip while minimizing tissue damage. Its fine design allows for use in narrow operative fields, typical of oral and periodontal surgery. As a Class I device, it meets the rigorous quality requirements for reusable surgical instrumentation, guaranteeing reliability during critical phases of holding or grasping soft tissues.

What are the clinical indications for this instrument?

This instrument is indicated for a multitude of actions in oral and implant surgery. Its main intended purpose is to allow the practitioner to maintain or grasp delicate tissues in an atraumatic manner. Beyond tissue manipulation, the Helmut Zepf micro surgical forceps is used to handle foreign bodies, hold sutures during knotting, or remove swabs during the operative act. Its specific 'Cooley' profile is particularly suited to interventions requiring great finesse, where preserving the integrity of anatomical structures is paramount for post-operative healing.

What are the technical characteristics of reference 22.815.17?

Technical reference 22.815.17 corresponds to a high-precision instrument developed by Helmut Zepf. Its main characteristic lies in its Cooley-type working part, designed for a firm but non-invasive grip. Manufactured from high-quality medical stainless steel, it possesses the necessary resistance to repeated decontamination cycles. Although delivered non-sterile, its design allows for thorough cleaning and sterilization, including the junction areas. The lightness and balance of the instrument are studied to reduce manual fatigue during prolonged reconstructive micro-surgery or implant surgery procedures.

What are the contraindications for the use of these forceps?

The main contraindication related to the use of this Helmut Zepf instrument is known hypersensitivity or intolerance to metals, particularly medical stainless steel. If a hypersensitivity reaction occurs in the patient upon contact with the instrument, the procedure must be immediately interrupted and appropriate medical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any intervention. Furthermore, the use of an instrument showing visible damage, such as cracks, breaks, or defects on the edges, is strictly prohibited to avoid any intraoperative risk.

What are the maintenance and reprocessing precautions?

Like any Class I surgical instrument, these forceps must follow a strict reprocessing protocol. Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The manufacturer emphasizes the importance of complete cleaning to remove any residue before sterilization. Before each intervention, a visual inspection is necessary to detect any wear or damage. Due to the materials used and the design of the instrument, there is no defined maximum limit for treatment cycles, as long as the functional and visual integrity of the forceps is preserved.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This device belongs to Class I according to medical device regulations. Compliance with manufacturing protocols ensures conformity with safety and performance requirements for manual surgical instruments. The use of this instrument is strictly reserved for qualified healthcare professionals. The manufacturer guarantees the traceability of its products via precise references, such as code 22.815.17, ensuring clinicians use equipment that complies with modern surgery standards.

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