INSTRUMENT SUPPORT - Helmut Zepf (85.181.04) - Delynov
The SUPPORT POUR INSTRUMENTS - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 85.181.04.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the Helmut Zepf instrument support?
The Helmut Zepf instrument support, bearing reference 85.181.04, is an instrumentation management device intended for dental practices and operating theaters. Designed by the manufacturer Helmut Zepf Medizintechnik GmbH, this support allows for structuring the layout of instruments in the INSTRU category. It primarily serves to maintain order and safety of medical devices during the various stages of handling, thus avoiding impacts between working parts and facilitating the workflow of the practitioner and their assistant during surgical interventions.
What are the clinical indications for this support?
This instrument support is indicated for the systematic organization of oral surgery, implantology, and periodontology trays. Its use is recommended for grouping instruments necessary for a specific procedure, allowing for rapid identification and ergonomic retrieval. In a clinical setting, it contributes to the optimization of the workspace on the surgical trolley. Although the source data does not specify exclusive protocols, this type of support is standard for the aseptic preparation and temporary storage of manual or rotary instruments before and after their use on the patient.
What are the technical characteristics of the 85.181.04 support?
The Helmut Zepf support reference 85.181.04 is distinguished by its design adapted to the requirements of sterilization and intensive clinical use. Although specific dimensions are not listed in the source data, this product belongs to the recognized range of Helmut Zepf Medizintechnik GmbH, specialized in high-end instrumentation. It is designed to accommodate several instruments simultaneously, ensuring their stability. Its structure allows for optimal exposure of surfaces to cleaning and sterilization agents, thus respecting the rigorous hygiene cycles imposed in dental surgery.
What are the contraindications for the use of this device?
There are no specific reported medical contraindications for the use of an instrument support, as this device does not come into direct and prolonged contact with patient tissues in an invasive manner. However, this support should not be used if it shows visible signs of corrosion, deformation, or structural damage that could compromise the stability of the instruments or the effectiveness of the sterilization process. Use must be strictly limited to the organization of instrumentation compatible with its dimensions and its fixation system.
What are the maintenance precautions for this Helmut Zepf support?
To ensure the longevity of the Helmut Zepf support, it is imperative to follow the decontamination and sterilization protocols recommended by the manufacturer Helmut Zepf Medizintechnik GmbH. After each intervention, the support must be cleaned to remove any organic residue. Although the exact material is not specified in the technical sheet, these devices are generally designed to withstand standard autoclave cycles. It is advisable to regularly inspect the 85.181.04 support to ensure the absence of residues in the instrument holding areas and to check the integrity of the device before each sterilization cycle.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized company in the dental and surgical instrumentation sector. Regarding standards and certifications, the regulatory class and CE marking are not specified in the current technical data for this product. It is therefore recommended that users systematically refer to the instructions for use and product labeling provided by the manufacturer to confirm compliance with the requirements of the European Medical Device Regulation (MDR) and to obtain specific safety instructions.
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Specialized surgical instrumentation is evolving towards ergonomic designs.



















