Universal PEEK handle - Helmut Zepf (26.194.13) - Delynov
The Manche universel en PEEK - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 26.194.13.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
Complete your order
Based on our customers' orders
What is the Helmut Zepf universal PEEK handle?
The universal PEEK handle, reference 26.194.13, is a dental instrumentation component manufactured by Helmut Zepf Medizintechnik GmbH. Made of PEEK (Polyetheretherketone), this high-performance polymer material is recognized for its lightness and resistance to repeated sterilization cycles. This dental handle is designed to receive various compatible inserts, thus allowing customization of instrumentation according to the needs of the surgical procedure. Its structure is designed to provide a stable and comfortable grip, meeting the requirements of professional use in dental practices or hospital environments.
What are the clinical indications?
This Helmut Zepf universal handle is indicated as a manual dental instrument for use during various clinical procedures. In oral, implant, or periodontal surgery, it serves as a support for diagnostic, scaling, or fine surgery instruments. Its use is strictly reserved for qualified healthcare professionals. It allows for the manipulation of active tips with the necessary precision during interventions on the soft or hard tissues of the oral cavity. The versatility of the universal system allows the instrumentation to be adapted to the specificity of each patient case, ensuring optimal flexibility during the operative protocol.
What are the technical characteristics?
The Helmut Zepf handle (reference 26.194.13) is distinguished by the use of PEEK, an advanced thermoplastic material. This technical choice ensures excellent dimensional stability and chemical resistance during reprocessing. Although the main body is made of PEEK, the manufacturer mentions the presence of medical stainless steel in the overall composition of its instruments, which guarantees the robustness of the assembly. The product is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient. The design allows compatibility with other products in the Helmut Zepf range, subject to prior verification.
What are the contraindications for use?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity to metals. Although the handle is primarily made of PEEK, contact with the instrument, which contains medical stainless steel, can trigger an allergic reaction or intolerance in certain patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and appropriate medical measures must be initiated. It is therefore crucial to evaluate the patient's allergic history before any use of this manual instrument in the mouth.
How is reprocessing carried out and what are the precautions?
Helmut Zepf products are delivered non-sterile. The safety protocol requires that each handle be cleaned, disinfected, and sterilized before initial commissioning and after each subsequent use. Before any use, the practitioner must perform a rigorous visual inspection to detect any damage or signs of wear such as cracks, breaks, or structural defects. The use of a damaged or worn product is formally prohibited. Due to the quality of the materials used and the design of the device, there is no defined maximum limit for treatment cycles, but the functional state of the instrument must remain the decision criterion for its continued service.
Who is the manufacturer and what standards are respected?
The official manufacturer of this universal handle is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing specifications). Compliance with cleaning and sterilization protocols is essential to guarantee patient safety and instrument longevity. As a Class I device, it meets the regulatory requirements in force for reusable manual dental instruments. Compatibility with other instruments in the Helmut Zepf system must be systematically verified by the healthcare professional before the surgical act.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.



















