Sinus Lift Spoon and Condenser Small Kirsch 7 - Helmut Zepf (41.868.07S) - Delynov
The Cuillère et fouloir combiné Sinus petit modèle Kirsch 7 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.868.07S.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Kirsch 7 Sinus combined spoon and plugger, small model?
The Kirsch 7 Sinus combined spoon and plugger, small model, is a precision surgical instrument designed by Helmut Zepf Medizintechnik GmbH. This double-ended device combines two essential functions into a single tool: a spoon part and a plugger part. Referenced under code 41.868.07S at Delynov, this small model is specifically sized for delicate interventions requiring fine manipulation of tissues or filling materials. Its ergonomic design allows practitioners to switch quickly from a curettage or harvesting action to a compacting action without changing instruments, thus optimizing the operative flow during surgical procedures.
What are the clinical indications for this Helmut Zepf instrument?
This Helmut Zepf combined instrument is primarily indicated for oral surgery and implantology, particularly for sinus lift procedures (sinus elevation). The spoon part facilitates access and manipulation of tissues or bone grafts, while the plugger part allows for precise compacting of bone substitute materials into prepared cavities. Its 'small model' format makes it particularly suitable for narrow anatomies or restricted access where high precision is required. It assists dental surgeons and implantologists in preparing the implant site and managing bone volumes during reconstruction phases.
What are the technical characteristics of the Kirsch 7 model (ref. 41.868.07S)?
The Kirsch 7 model, identified by technical reference 41.868.07S, is distinguished by its double working configuration. As a combined instrument, it integrates a spoon-type active end and a plugger-type end. Manufactured by Helmut Zepf, this tool benefits from the high-quality finish characteristic of the German brand's standards. Although exact dimensions are not specified beyond the 'small model' designation, its structure is optimized for robustness and durability in a surgical environment. The monoblock design ensures direct force transmission and excellent tactile sensation during sinus grafting maneuvers.
What are the contraindications for using this sinus instrument?
The use of the Kirsch 7 Sinus combined spoon and plugger is contraindicated whenever clinical conditions do not allow for standard oral surgical intervention (untreated infections, severe systemic pathologies contraindicating surgery). The instrument must not be used for applications diverted from its primary function of manipulating soft tissues or bone filling materials. The practitioner must ensure that the size of the instrument is compatible with the workspace to avoid any iatrogenic trauma. As with any reusable instrument, non-compliant sterilization constitutes a major contraindication to its use in the operating room.
What are the maintenance precautions for this Helmut Zepf instrument?
To guarantee the longevity of the Helmut Zepf instrument, it is imperative to follow the cleaning, disinfection, and sterilization protocols recommended by the manufacturer Helmut Zepf Medizintechnik GmbH. After each intervention, the instrument must be cleared of filling material residues or tissue. Non-corrosive cleaning solutions suitable for metallic surgical instruments should be used. Particular attention must be paid to the ends (spoon and plugger) to avoid shocks that could alter the precision of the active parts. A visual inspection of the integrity of reference 41.868.07S is recommended before each sterilization cycle.
Who is the manufacturer and what standards are met by this device?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a globally recognized player for the quality of its dental and surgical instrumentation. Regarding specific standards, the CE marking and regulatory class are not explicitly detailed in the current technical data for this reference 41.868.07S. However, as a European manufacturer of medical devices, Helmut Zepf subjects its products to the safety and performance requirements in force. Healthcare professionals are invited to systematically consult the instructions for use and labeling provided with the product to verify certifications and reprocessing instructions compliant with local regulations.
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| Manufacturer | Helmut Zepf |
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