Double Bone Grafting Material Applicator - Helmut Zepf (19.603.10) - Delynov
The Applicateur double pour matériel d'augmentation osseuse - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.603.10.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf double applicator (19.603.10)?
The Helmut Zepf double applicator, referenced under code 19.603.10, is a manual instrument specifically designed for handling filling materials in oral surgery. This device functions as a bone graft carrier equipped with two functional ends, allowing for efficient management of biomaterials. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is intended for practitioners performing bone reconstruction procedures. Its structure is optimized for loading, transporting, and depositing augmentation material directly into the surgical area, offering a technical alternative to the use of simple curettes or standard dental bone syringes.
What are the clinical indications for this instrument?
This instrument is indicated for all bone surgery procedures requiring the addition of exogenous or autologous materials. It is particularly used during ridge augmentations, the filling of periodontal defects, or sinus lifts. As a biomaterial applicator, it allows for the precise placement of granules or crushed bone into difficult-to-access cavities. Its use is common in implantology to stabilize bone volume around implants or to fill the socket after an extraction. Its double end offers appreciated versatility to adapt to the morphology of the recipient site during bone grafts.
What are the technical characteristics of this applicator?
The Helmut Zepf applicator (19.603.10) is distinguished by its double configuration. Although specific dimensions are not detailed, its design is based on the expertise of Helmut Zepf Medizintechnik GmbH in high-precision surgical instrumentation. This bone surgery instrument is designed to withstand the cleaning and sterilization cycles required in a dental office. The surface finish is developed to prevent excessive adhesion of biomaterials, thereby facilitating their release into the graft site. Reference 19.603.10 corresponds to a specific model within the manufacturer's bone augmentation range, ensuring ergonomics adapted to the fine movements of micro-surgery.
What are the contraindications for the use of this device?
There are no specific medical contraindications intrinsically linked to the use of this manual instrument, other than those related to the surgical act itself or the patient's general state of health (coagulation disorders, uncontrolled systemic pathologies). However, the use of this bone graft applicator must be avoided if the instrument shows visible signs of degradation, corrosion, or bending, which could compromise the safety of the procedure or the integrity of the tissues. The practitioner must ensure the compatibility of the tip size with the particle size of the material used to avoid any blockage or imprecise application.
What are the maintenance precautions for this instrument?
Like any reusable surgical instrument from the Helmut Zepf brand, this applicator must be subjected to a rigorous protocol of decontamination, cleaning, and autoclave sterilization after each use. It is necessary to strictly follow the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH regarding compatible cleaning products to preserve the surface condition of the steel. Particular attention must be paid to the ends of the applicator to remove any dried biomaterial residue before sterilization. Regular visual inspection is necessary to check for the absence of premature wear, thus ensuring the longevity of this instrument in the implant surgery arsenal.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a company recognized for the quality of its surgical instrumentation. Regarding standards and certifications, this product is manufactured according to German industrial quality standards. To obtain precise information on the regulatory class of the device, its CE marking, or its compliance with the European Medical Device Regulation (MDR), it is imperative to refer to the product labeling and the instructions for use provided by Helmut Zepf. The manufacturer is committed to providing devices that meet safety and performance requirements for use in a professional surgical environment.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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