x1 impression tray for Benex (BE001 090) - Meisinger - Hager & Meisinger GmbH (47BE001230090) (47BE001230090) - Delynov

What is the Meisinger impression tray for Benex?

The impression tray for Benex (reference 47BE001230090) is a specialized instrument developed by the manufacturer Hager & Meisinger GmbH. This device is designed to accompany the Benex extraction system, a recognized tool in oral surgery for atraumatic extractions. This impression tray allows for the precise capture of the morphology necessary for the proper functioning of the system or for post-extraction planning. As a product of the Meisinger brand, it benefits from a rigorous design meeting the requirements of the strictest surgical environments, ensuring perfect compatibility with other components of the Benex range for optimal clinical efficiency during each intervention.

What are the clinical indications for this device?

The tooth extraction impression tray is indicated for complex surgical procedures where the use of the Benex system is required. It is primarily used in maxillary surgery and implantology to facilitate precise impression taking before or during extraction. According to the guidelines of the manufacturer Hager & Meisinger GmbH, the use of this type of device assumes adequate expertise and experience in diagnosis, preoperative planning, and surgical techniques. The physician decides, under their sole and entire responsibility, on the use of this Meisinger instrument on a case-by-case basis, depending on the patient's particular clinical situation and the specific extraction indication.

What are the technical characteristics of the impression tray (BE001 090)?

The benex impression tray, bearing the technical reference 47BE001230090, is a precision instrument manufactured by Hager & Meisinger GmbH. This device is classified as a Class IIa surgical instrument, guaranteeing a high level of control for patient safety. It bears the CE0044 marking, attesting to its compliance with current European standards. Its design is specifically adapted to fit the components of the Benex kit (BE001 090). It is imperative that this instrument be used in accordance with its intended purpose to avoid premature wear or risk to the user, as emphasized by the manufacturer in its official technical documentation.

What are the contraindications for the use of this instrument?

Although the raw MDR text does not specify direct medical contraindications related to composition, it highlights crucial usage restrictions. The use of the extraction impression tray is strictly reserved for dentists, physicians, or specialists with solid training and experience in the relevant disciplines, such as implantology or maxillary surgery. Use that does not comply with the Meisinger manufacturer's specifications can lead to risks for patients and premature wear of the equipment. The practitioner must evaluate each clinical situation individually to determine if the patient's condition or anatomical configuration allows for the safe use of this surgical device.

What are the precautions for use and maintenance?

To guarantee the longevity of the benex impression tray and the safety of care, it is essential to follow the recommendations of Hager & Meisinger GmbH. Any non-compliant use may involve risks for patients and users. The manufacturer recommends referring to the catalog for detailed information on possible applications and regularly participating in the continuing education sessions offered. In the event of a serious incident occurring in connection with the device, it is mandatory to notify the manufacturer as well as the competent authority of the Member State. Particular attention must be paid to cleaning and sterilization, in accordance with standard protocols for reusable Class IIa medical devices.

Who is the manufacturer and what standards are respected?

The impression tray for Benex is manufactured by Hager & Meisinger GmbH, a company based in Neuss, Germany. This recognized manufacturer complies with the strictest European regulatory standards, as evidenced by the CE0044 marking affixed to the product. The device is classified as Class IIa according to the Medical Device Regulation (MDR). Meisinger ensures rigorous monitoring of the quality of its products and provides healthcare professionals with detailed information via their website and catalogs. Compliance with these standards guarantees dental surgeons and implantologists a reliable, secure instrument perfectly adapted to the requirements of modern oral surgery.

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Surgical medical consumables play a decisive role in operative safety.