Universal surgical PEEK handle for M4x0.5 mm interchangeable inserts - Helmut Zepf (26.193.07) - Delynov
The Manche universel chirurgical en PEEK, pour inserts échangeables M4x0,5 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 26.193.07.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the Helmut Zepf universal surgical PEEK handle?
The universal surgical PEEK handle, referenced under code 26.193.07 by Helmut Zepf, is an instrument designed to serve as a support for interchangeable inserts. Its main structure is manufactured from PEEK (Polyetheretherketone), a technical polymer recognized in the medical field for its mechanical properties and resistance. This universal peek handle is equipped with an M4x0.5 mm thread fixation system, allowing the adaptation of different types of working tips according to the needs of the intervention. Its ergonomic design facilitates the practitioner's grip during technical gestures in dental surgery.
What are the clinical indications for this insert holder handle?
This surgical instrument handle is primarily indicated for oral surgery, periodontology, and implantology procedures requiring the use of removable inserts. It serves as a gripping base for diagnostic, measurement, or specific work tools on hard and soft tissues. In implant surgery, it allows for the precise manipulation of inserts compatible with the M4x0.5 mm screw pitch. Its versatility makes it a central tool for practitioners wishing to streamline their instrumentation while maintaining high modularity during the different operative phases in a dental office or surgical suite.
What are the technical characteristics of the m4 peek handle?
The m4 peek handle features precise technical specifications to meet the requirements of modern surgery. Its major characteristic is its M4x0.5 mm female thread, which ensures a stable and rigid connection with compatible Helmut Zepf inserts. The choice of PEEK as a construction material offers an alternative to traditional metal handles while guaranteeing excellent durability. The technical reference 26.193.07 corresponds to a manufacturing standard from Helmut Zepf Medizintechnik GmbH, ensuring perfect compatibility with the accessories intended for this universal mounting system.
What are the contraindications for the use of this instrument?
The contraindications related to the use of this universal dental surgery handle mainly concern non-compliance with sterilization protocols or use with non-compatible inserts. It must not be used if the M4x0.5 mm thread shows signs of wear or deformation that could compromise the fixation of the insert. Additionally, using this instrument for tasks exceeding its mechanical capacities intended by Helmut Zepf is prohibited. It is the practitioner's responsibility to check the integrity of the PEEK material before each intervention to ensure the absence of cracks or structural degradation.
What are the maintenance precautions for PEEK material?
Although PEEK is a highly resistant material, the maintenance of this surgical handle requires particular attention to guarantee its longevity. It must be cleaned and sterilized in accordance with the instructions provided by the manufacturer Helmut Zepf Medizintechnik GmbH. Practitioners must use appropriate cleaning solutions that do not alter technical polymers. It is recommended to systematically check the cleanliness of the internal M4x0.5 mm thread to avoid any accumulation of biological debris that could hinder the screwing of the inserts. Rigorous drying after each sterilization cycle is recommended to maintain the physical properties of the handle.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-precision surgical instrumentation. This universal handle is designed according to the rigorous quality standards of the German brand. Regarding specific certifications such as the regulatory class or CE marking, this information must be verified directly on the product labeling or in the technical documentation provided by Helmut Zepf, as they are not specified in the current source data. Compliance with the use and maintenance protocols defined by the manufacturer is essential to guarantee the conformity of the device during its clinical use.
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