PROPHYLAXIS KIT. Z-SHAPE RELAX HANDLE. INCLUDING: - Helmut Zepf (24.989.55OX) - Delynov
The KIT DE PROPHYLAXIE. MANCHE Z-SHAPE RELAX. COMPRNANT: - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.989.55OX.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the KIT DE PROPHYLAXIE MANCHE Z-SHAPE RELAX?
The KIT DE PROPHYLAXIE MANCHE Z-SHAPE RELAX, referenced under code 24.989.55OX by Helmut Zepf, is a set of manual instruments specifically developed for periodontal care. This kit is distinguished by the use of the Z-Shape Relax handle, designed by Helmut Zepf Medizintechnik GmbH to offer an ergonomic configuration during cleaning interventions. The instruments are manufactured from high-quality medical stainless steel, guaranteeing the robustness necessary for prophylaxis acts in the dental office. This device is delivered non-sterile and requires a complete protocol of cleaning, disinfection, and sterilization before its first use and between each patient.
What are the clinical indications for this kit?
This scaling instrument kit is indicated for interventions on the dental apparatus as part of complete periodontal treatments. Its primary use consists of accurately probing gingival pockets to assess the health status of the periodontium. Furthermore, the included instruments allow for the mechanical removal of tartar, whether soft (bacterial plaque) or hard (calculus), on dental surfaces or dental appliances. It constitutes an indispensable dental hygiene instrumentation solution for scaling and manual root planing phases, allowing for meticulous cleaning of difficult-to-access areas.
What are the technical characteristics of the Helmut Zepf kit?
Technically, this Helmut Zepf kit is based on medical stainless steel manufacturing, a material chosen for its resistance to repeated sterilization cycles. Reference 24.989.55OX integrates the specific Z-Shape Relax handle, which modifies the grip axis to adapt to hand constraints during scraping and probing movements. According to the manufacturer's data, there is no defined maximum limit for the number of processing cycles achievable, as the lifespan depends on the design, materials, and observed wear. Each instrument must be visually inspected for potential cracks or defects on the cutting edges before any use.
What are the contraindications for the use of these instruments?
The main medical contraindication concerns known hypersensitivity or intolerance to metals. Contact between the medical stainless steel instrument and the patient's tissues may trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf Medizintechnik GmbH stipulates that the intervention must be immediately stopped and necessary medical measures must be taken. Additionally, use is strictly contraindicated if the instrument shows visible damage such as breaks, cracks, or excessive wear of the working parts, in order to guarantee patient safety.
What are the maintenance and reprocessing precautions?
As Helmut Zepf products are delivered non-sterile, a complete reprocessing cycle is mandatory before the first use. This includes cleaning, disinfection, and sterilization. It is imperative to check compatibility with other cleaning products used in the office. Before each subsequent use, the instrumentation must undergo the same rigorous protocol. The practitioner must systematically check for the absence of defects on the cutting edges. Since these are non-resorbable steel instruments, their physical integrity is the only end-of-life criterion, with no cycle limit technically imposed by the manufacturer as long as the device does not show wear compromising its use.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This prophylaxis kit is classified as a Class I medical device according to current regulations. As a Class I device, it meets the safety and performance requirements defined for this category of manual dental instruments. Compliance with the manufacturer's safety instructions, particularly regarding systematic cleaning and sterilization, is essential to maintain product conformity during its use by qualified healthcare professionals.
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Specifications
| Manufacturer | Helmut Zepf |
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