Rack for Benex extraction system - Helmut Zepf (12.302.01) - Delynov
The Rack pour système d'extraction Benex - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 12.302.01.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the rack for the Benex - Helmut Zepf extraction system?
The rack for the Benex extraction system, referenced under code 12.302.01, is a support device designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This benex support is specifically developed to accommodate the various technical components necessary for the implementation of the root extraction system. It is an organizational accessory intended for oral surgery technical platforms, allowing each element to be kept in its defined place. Its structure is adapted to the requirements of cleaning and equipment management in dental practices, ensuring that the benex extraction system remains complete and ready for use for each intervention.
What are the clinical indications for this support?
The use of this benex rack is indicated during all surgical procedures requiring the use of the atraumatic extraction system from Helmut Zepf. In implant and oral surgery, the preservation of the socket and the vestibular bone plate is crucial. This rack allows the practitioner to have all the extraction tools (screws, extractors, supports) available in an organized manner. It is particularly useful during extractions of fractured or deeply impacted roots where rapid access to the Benex system components optimizes the clinical workflow and the management of the operative field.
What are the technical characteristics of the 12.302.01 rack?
The rack for the Benex extraction system (reference 12.302.01) is characterized by a design specifically adapted to the morphology of Helmut Zepf parts. Although exact dimensions are not specified, its configuration allows for stable maintenance of the instruments during transport and storage. As part of the benex extraction system, this rack is designed to withstand standard decontamination cycles applied to medical devices in dentistry. Its design facilitates immediate visual identification of missing components, thus ensuring rigorous management of the instrumental inventory before and after each surgical act.
What are the contraindications for the use of this rack?
There are no direct medical contraindications related to the use of this storage rack, as it does not come into direct contact with the patient's tissues in an invasive manner. However, its use is strictly limited to the storage and organization of the Benex extraction system from Helmut Zepf. Using this rack for incompatible instruments or those not designed for its specific slots could lead to equipment instability or damage to the instruments. It is advisable to systematically refer to the manufacturer's sterilization protocols to avoid any degradation of the support or the instruments it contains.
What are the maintenance precautions for this equipment?
The benex extraction rack must be maintained according to the cleaning, disinfection, and sterilization protocols recommended by Helmut Zepf Medizintechnik GmbH. Like any surgical instrumentation support, it must be cleared of any organic residue after use. Although material specifications are not detailed, this type of rack is generally designed to withstand autoclave cycles. It is recommended to check the integrity of the support regularly to ensure that the maintenance of the benex extraction system components remains optimal and secure for the practitioner and their team.
Who is the manufacturer and what standards are met?
The rack for the Benex extraction system is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-precision dental surgical instrumentation. The technical reference for this product is 12.302.01. Regarding standards and certifications, although the regulatory class and specific CE marking are not mentioned in the technical documentation provided, the product comes from the rigorous manufacturing processes of Helmut Zepf. For any precise information on compliance with the Medical Device Regulation (MDR) or ISO certifications, it is advisable to consult the instructions for use or the certificates of conformity provided by the manufacturer.
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Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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