Bone Crushing Forceps - Helmut Zepf (47.958.00) - Delynov
The Tenailles pour broyer l'os - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 47.958.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf bone crushing forceps?
The Helmut Zepf bone crushing forceps, referenced under code 47.958.00, is a manual surgical instrument specifically designed for the manipulation of hard tissues in oral surgery. Manufactured from high-quality medical stainless steel, these bone crushing pliers allow for the fragmentation of autologous bone harvests. Its robust structure is adapted to the mechanical stresses required to reduce bone material into usable particles. This device belongs to the category of reusable consumables (CONSO) and benefits from the expertise of Helmut Zepf Medizintechnik GmbH in the design of precision tooling for healthcare professionals.
What are the clinical indications for this manual bone crusher?
The primary indication for this manual bone crusher is the grinding of autologous bone material harvested intra-orally. In implant and periodontal surgery, it is common to harvest bone fragments from donor sites for reuse at recipient sites presenting volumetric deficits. The use of these surgical bone forceps allows for obtaining a grain size suitable for bone grafting, thus facilitating the placement of the material and potentially promoting osseointegration processes. The instrument is exclusively reserved for use by qualified healthcare professionals proficient in guided bone regeneration protocols.
What are the technical characteristics of the Helmut Zepf 47.958.00 forceps?
The Helmut Zepf bone forceps are characterized by their full medical stainless steel construction, ensuring corrosion resistance and durability during sterilization cycles. Identified by technical reference 47.958.00, it features cutting edges designed to efficiently crush mineralized structures. As a Class I device, it meets regulatory safety requirements. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit for the number of processing cycles, although wear must be visually checked before each intervention.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of these bone crushing pliers concerns the patient's known hypersensitivity to metals. Since the instrument is composed of medical stainless steel, contact can trigger an allergic reaction in intolerant subjects. If such a hypersensitivity reaction occurs during the procedure, the manufacturer Helmut Zepf stipulates that the intervention must be immediately stopped and necessary medical measures must be taken. Furthermore, use is contraindicated if the instrument shows visible damage such as cracks, breaks, or defects on the cutting edges, to ensure patient safety and the effectiveness of the surgical procedure.
What are the maintenance and sterilization precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and require a strict protocol before any use. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to check for the absence of visible damage and wear, such as cracks or defects on the cutting parts, before each surgical act. Any damaged or worn product must never be used. Reprocessing must be complete to ensure microbiological safety, and compatibility with other products used simultaneously must be verified beforehand by the practitioner.
Who is the manufacturer and what standards are met?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects rigorous quality standards for medical devices. The bone crushing forceps are classified as a Class I medical device according to current regulations. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Each production step, from the choice of medical stainless steel to the finishing of reference 47.958.00, is controlled to ensure compliance with the safety and performance requirements expected in oral surgery.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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