Mid Straight Long Silver t - 0.6 4Holes - JEIL Medical

What is the Mid Straight Long Silver t - 0.6 4Holes from Jeil Medical?

The Mid Straight Long Silver t - 0.6 4Holes is a technical device designed by Jeil Medical for specialized surgical interventions. This product, identified under reference 242.21ST04, features a long straight configuration (Mid Straight Long) with a structure comprising 4 perforations (4Holes). Developed by Jeil Medical Corp., this component belongs to the surgical consumables category. Its specific design meets the precision needs of oral and maxillofacial surgery practitioners, offering a solution adapted to demanding clinical protocols.

What are the clinical indications for this device?

The Mid Straight Long Silver t - 0.6 4Holes from Jeil Medical is primarily indicated for oral surgery, implantology, or bone reconstruction procedures requiring the use of plates or support brackets. Although specific manufacturer data does not detail every application, this type of 4-hole device is conventionally used for stabilization and fixation during precise surgical maneuvers. It allows dental surgeons and implantologists to perform reliable mechanical assemblies within the oral cavity.

What are the technical characteristics of product 242.21ST04?

The technical characteristics of the Jeil Medical product are based on its geometry and specific reference. It is a 'Mid Straight Long' model with a thickness or technical parameter of 0.6. The presence of 4 holes (4Holes) allows for modularity during placement and fixation adapted to the anatomical constraints encountered. Reference 242.21ST04 ensures product traceability within the Jeil Medical Corp. range. Its 'Silver' finish and elongated straight shape facilitate its integration into surgical sites with complex access.

What are the contraindications for the use of this material?

Contraindications for the use of the Mid Straight Long Silver t - 0.6 4Holes include any known hypersensitivity to the materials constituting the device, although the exact composition is not specified here. Generally, use is discouraged in cases of active infection at the surgical site, insufficient vascularization, or severe systemic pathologies that could compromise bone or mucosal healing. It is the practitioner's responsibility to evaluate the benefit/risk ratio based on the patient's general health status and the recommendations provided in the manufacturer's instructions for use.

What are the precautions for use and handling?

When handling the Jeil Medical device (reference 242.21ST04), it is imperative to respect strict aseptic conditions to avoid any risk of cross-contamination. The surgeon must ensure not to alter the structure of the device (the 4 holes and the straight part) during placement, in order to maintain the mechanical integrity of the assembly. Particular attention must be paid to the quality of the receiving bone support. After the intervention, regular clinical follow-up is necessary to monitor the integration of the device and the absence of adverse inflammatory reactions.

Who is the manufacturer and what standards are met?

The device is manufactured by Jeil Medical Corp., a recognized player in the field of surgical instrumentation and devices. Regarding safety standards, the CE marking and the specific regulatory class are not detailed in the available sources for this reference 242.21ST04. Healthcare professionals are therefore invited to systematically consult the product labeling as well as the technical instructions provided by Jeil Medical to verify current certifications, sterilization protocols, and compliance with local regulatory requirements before any use.

State of the art

Surgical medical consumables play a decisive role in operative safety.