X-Guide storage cassette with X-Mark slot (Made in France) (PS502133) - Delynov
The Cassette de rangement X-Guide avec logement X-Mark (Made in France) is a medical device manufactured by X-Nav Technologies LLC.
- Manufacturer: X-Nav Technologies LLC.
- Reference: PS502133.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the X-Guide storage tray with X-Mark slot?
The X-Guide storage tray, referenced under code PS502133 by Delynov, is an instrument management device specifically developed for the surgical navigation ecosystem of X-Nav Technologies LLC. This French-made product is designed to accommodate the elements necessary for computer-assisted interventions. Its structure integrates a specific slot for the X-Mark, allowing for rigorous organization of the technical platform. As an instrument storage tray, it facilitates the workflow in oral surgery by grouping critical components in a single, structured receptacle.
What are the clinical indications for this X-Nav device?
The use of this tray is indicated within the framework of implant and oral surgery using the X-Guide dynamic navigation system from X-Nav. It serves as logistical support for practitioners performing real-time guided implant placements. The device allows for the securing of specific equipment, notably the X-Mark marker, before, during, and after the surgical act. Its use is part of a clinical procedure standardization approach, aiming to maintain the integrity of technological components essential for surgical navigation precision within the dental office or clinic.
What are the technical characteristics of the PS502133 tray?
The X-Guide storage tray is distinguished by its technical reference PS502133 and its 'Made in France' design. It is configured with precise locations, including a dedicated slot for the X-Mark, ensuring that each part of the X-Nav system remains immobile and protected. Although the exact materials are not specified in the source data, this type of surgical storage tray is generally designed to withstand the constraints of surgical environments. Its configuration is optimized for navigation equipment management, ensuring perfect compatibility with the instrument dimensions of the manufacturer X-Nav Technologies LLC.
What are the contraindications for the use of this tray?
There are no direct medical contraindications related to the use of this storage tray, as it does not come into direct and permanent contact with the patient's biological tissues. However, its use is strictly limited to the storage and organization of compatible instruments from the X-Nav system. Using this tray for unsuitable instruments or competing brands could compromise the secure holding of the parts. Practitioners must systematically refer to the cleaning and sterilization protocols provided by X-Nav Technologies LLC to avoid any degradation of the device or risk of cross-contamination.
What are the maintenance precautions for this storage equipment?
As a non-resorbable device intended for instrumental organization, the precautions for use are based on compliance with decontamination and sterilization cycles. The instrument storage tray must be inspected regularly to check for the absence of residues or structural damage that could harm the protection of the X-Mark or other X-Nav components. It is imperative to follow the manufacturer's recommendations regarding compatible cleaning agents to preserve the product's longevity. Careful handling during the opening and closing of the case is advised to maintain the precise fit of the internal slots.
Who is the manufacturer and what standards are respected?
The X-Guide storage tray with X-Mark slot is manufactured by X-Nav Technologies LLC, a recognized manufacturer in the field of surgical navigation. This product benefits from French manufacturing, highlighting a commitment to local production quality. Regarding regulatory standards, the class and CE marking are not specified in the current technical documentation. Healthcare professionals are invited to consult the product labeling and the instructions for use provided by the manufacturer to obtain detailed information on regulatory compliance and specific certifications in force for this CONSO category device.
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