GRAFT AND SINUS PACKER WITH INTERCHANGEABLE INSERTS AND HANDLE - Helmut Zepf (47.848.03) - Delynov
The GRAFT AND SINUS PACKERINSERTS ÉCHNAGEABLES AVEC MANCHE- Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 47.848.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf GRAFT AND SINUS PACKER?
The Helmut Zepf GRAFT AND SINUS PACKER, bearing reference 47.848.03, is a specialized surgical instrument designed for implantology and periodontal surgery. This device consists of an ergonomic handle and exchangeable inserts, offering increased flexibility during bone grafting procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is specifically developed to handle graft materials with high technical rigor. Its modular structure allows practitioners to select the tip most suited to the morphology of the recipient site, thus ensuring precise application of the biomaterial in sometimes complex access areas.
What are the clinical indications for this instrument?
This instrument is primarily indicated during sinus floor elevation surgeries, commonly known as sinus lifts, as well as for alveolar ridge augmentations. As a dental sinus packer, it is used to gently compact bone substitute material under the previously lifted sinus membrane. It is also used as a dental graft packer to densify the graft in peri-implant bone defects or extraction sockets. Its use is reserved for dental surgeons and oral surgery specialists practicing pre-implant bone reconstruction procedures requiring precise tactile control during the condensation phase.
What are the technical characteristics of model 47.848.03?
The Helmut Zepf model 47.848.03 is distinguished by its system of interchangeable inserts mounted on a dedicated handle. This technical configuration allows for varying the diameters and shapes of the working tips without multiplying the number of complete handles. The design of the instrument aims to ensure optimal force transmission during the compacting of bone particles or synthetic substitutes. Although the specific dimensions of the inserts are not detailed here, the technical reference guarantees compatibility between the components of the Helmut Zepf Medizintechnik GmbH system, ensuring perfect stability of the insert once fixed on the handle for maximum operative safety.
What are the contraindications for the use of this instrument?
The contraindications for using the GRAFT AND SINUS PACKER are essentially related to the general contraindications of oral and implant surgery. The use of this instrument is prohibited if the patient presents uncontrolled systemic pathologies preventing any surgical intervention. Furthermore, it must not be used if the surgical site presents an untreated acute infection or if the sinus membrane is irreparably damaged, making filling impossible. It is also necessary to ensure the absence of known allergy to the metallic components of the instrumentation. The choice of instrument must always result from a thorough clinical diagnosis and adequate preoperative planning.
What are the maintenance precautions for this Helmut Zepf device?
Like any precision surgical instrument manufactured by Helmut Zepf Medizintechnik GmbH, the GRAFT AND SINUS PACKER requires a rigorous decontamination and sterilization protocol after each use. It is imperative to disassemble the exchangeable inserts from the handle before cleaning to remove any biomaterial residue or organic debris in the threads. Cleaning must be carried out with appropriate enzymatic solutions, followed by thorough rinsing and complete drying. Steam autoclave sterilization is the standard method, following the cycles recommended by the manufacturer. Inadequate maintenance can compromise the longevity of the insert fixation mechanism and the integrity of the instrument.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-quality dental instrumentation. Production follows strict manufacturing processes to guarantee the reliability of devices intended for oral surgery. Although the specific regulatory class and CE marking are not explicitly mentioned in the source data for this reference 47.848.03, Helmut Zepf products are designed to meet the technical requirements of modern clinical practice. Practitioners are invited to refer to the instructions for use and product labeling to verify current certifications and the manufacturer's specific recommendations regarding compliance with international standards.
State of the art
Single-use sterile surgical kits significantly reduce intraoperative contamination.
Specifications
| Manufacturer | Helmut Zepf |
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