Micro Self Tapping Gold OD - 1.3 L - 5 - JEIL Medical
The Micro Self Tapping Gold OD - 1.3 L - 5 - JEIL Medical is a medical device manufactured by Jeil Medical Corp..
- Manufacturer: Jeil Medical Corp..
- Reference: 241.011305.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Micro Self Tapping Gold OD - 1.3 L - 5 - Jeil Medical?
The Micro Self Tapping Gold OD - 1.3 L - 5 is a specialized device designed by Jeil Medical for guided bone regeneration (GBR) procedures. This technical component, identified under reference 241.011305, is distinguished by its self-tapping design, facilitating its insertion during surgical interventions. As a product developed by Jeil Medical Corp, it is part of a rigorous bone fixation protocol. Its specific structure is designed to meet the primary stability requirements necessary in oral and implant surgery, offering practitioners a reliable solution for maintaining grafts or membranes during reconstruction phases.
What are the clinical indications for this Jeil Medical product?
This Micro Self Tapping Gold OD device is primarily indicated for use in oral, dental, and implantology surgery. It is used by specialized surgeons for guided bone regeneration (GBR) procedures requiring precise and stable fixation. Its use is recommended for maintaining structures during bone volume augmentation or the stabilization of barrier devices. Thanks to its self-tapping technology, it allows for efficient application at recipient sites, thus ensuring the success of bone reconstruction protocols before or during dental implant placement.
What are the technical characteristics of product 241.011305?
The device referenced 241.011305 by Jeil Medical features precise technical characteristics extracted from its name: a diameter of 1.3 and a length of 5 (L - 5). The 'Gold OD' designation indicates a specific finish unique to the Jeil Medical Corp range. Its 'Self Tapping' property is a major feature, allowing the device to create its own thread during insertion, which optimizes operative time and mechanical hold in the bone. These specifications are essential for dental surgeons and implantologists seeking high-precision instrumentation for their GBR interventions.
What are the contraindications for the use of this GBR device?
Although specific data are not detailed here, general contraindications for this type of fixation device in oral surgery include uncontrolled systemic pathologies affecting bone metabolism or healing. It is imperative not to use this product if the patient has a known hypersensitivity to the manufacturing materials. Practitioners must evaluate the residual bone quality to ensure the stability of the device. For any clarification regarding specific contraindications related to composition or clinical use, it is essential to systematically refer to the technical instructions provided by the manufacturer Jeil Medical Corp.
What precautions should be taken during use?
The use of the Micro Self Tapping Gold OD requires technical expertise in implant surgery and bone regeneration. Precautions for use include careful handling of the device to preserve the integrity of the self-tapping thread during insertion. The surgeon must ensure the appropriate tightening torque to avoid any material fracture or bone site injury. As with any non-resorbable device intended for fixation, rigorous post-operative monitoring is necessary to prevent any infectious complications or exposure of the material. Compliance with sterility protocols and Jeil Medical instructions is crucial for patient safety.
Who is the manufacturer and what standards are met?
This device is manufactured by Jeil Medical Corp., a recognized player in the field of medical devices for maxillofacial and dental surgery. The product is distributed by Delynov under reference 241.011305. Regarding manufacturing standards, regulatory certifications, and CE marking, this information is not specified in the current technical sheet. Healthcare professionals are strongly encouraged to consult the product labeling and official documentation from the manufacturer Jeil Medical to verify the risk class and compliance with current regulatory requirements before any use in the office or operating room.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | JEIL MEDICAL |
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