Mini Friedman Bone Gouge Forceps 14cm 30 degrees - Helmut Zepf (42.320.14) - Delynov
The Pince-Gouge Mini Friedman 14 cm 30 degrés - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 42.320.14.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Mini Friedman 14 cm bone rongeur?
The Mini Friedman 14 cm bone rongeur, referenced under code 42.320.14 by Helmut Zepf Medizintechnik GmbH, is a precision instrument designed for fine bone surgery. Manufactured from medical stainless steel, it consists of two cutting jaws activated by stable shafts allowing for a bone cutting or crushing action. Its compact 14 cm structure and specific 30-degree tilt make it a tool particularly suited for interventions in difficult-to-access areas. As a Class I device, this instrument meets the quality requirements necessary for short-term invasive surgical procedures in dental offices or hospital environments.
What are the clinical indications for this bone surgical forceps?
This bone surgical forceps is mainly indicated for bone remodeling and regularization of alveolar ridges. In oral surgery, it is used during alveoloplasty procedures to remove protruding bone spicules after an extraction, thus facilitating gingival healing. In implantology, it allows for the preparation of the recipient site by removing bone irregularities or exostoses that could interfere with the positioning of soft tissues or prosthetic components. Its clean cutting action is essential for obtaining a smooth and clean bone surface, promoting optimal integration of graft materials or implants.
What are the technical characteristics of reference 42.320.14?
The Mini Friedman bone rongeur from Helmut Zepf features rigorous technical specifications to meet the needs of practitioners. It has a total length of 14 cm, offering sufficient leverage for bone cutting while maintaining great maneuverability. The working part is inclined at 30 degrees, a fundamental characteristic for improving visibility and access to the posterior sectors of the oral cavity. The instrument is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient, in accordance with current reprocessing protocols.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this instrument is the patient's known hypersensitivity or intolerance to metals, specifically to the medical stainless steel used in the composition of the device. A hypersensitivity reaction can be triggered during contact between the instrument and the patient's tissues. The manufacturer states that if such a reaction occurs, the surgical procedure must be immediately interrupted and the necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any intervention involving the use of this bone rongeur.
What are the maintenance and reprocessing precautions?
Like any Class I reusable surgical instrument, the Helmut Zepf bone rongeur requires strict maintenance. Before each use, the practitioner must visually inspect the instrument for any damage such as cracks, breaks, or wear of the cutting edges. It is strictly forbidden to use a damaged product. The reprocessing process includes cleaning, disinfection, and sterilization. Due to the robust design and materials used by Helmut Zepf, there is no defined maximum limit of treatment cycles, provided that the functional integrity of the instrument is preserved and verified before each procedure.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product belongs to Class I of medical devices according to current regulations. It is designed exclusively for use by qualified healthcare professionals. Compliance with manufacturing standards guarantees the use of medical stainless steel conforming to surgical requirements. Helmut Zepf ensures the traceability of its instruments, identifiable by their reference code 42.320.14, thus guaranteeing the safety and compliance of the equipment used within dental and oral surgery operating blocks.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Helmut Zepf |
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