Self-tapping silver plated screw tap - 1.6 L - 5 - JEIL Medical (241.011605) - Delynov
The Vis auto-taraudeuse argentée OD - 1,6 L - 5 - JEIL Medical is a medical device manufactured by Jeil Medical Corp..
- Manufacturer: Jeil Medical Corp..
- Reference: 241.011605.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Jeil Medical silver self-tapping screw OD 1.6 L 5?
The Jeil Medical silver self-tapping OD screw is a micro-osteosynthesis device used in oral surgery. Featuring a diameter of 1.6 mm and a length of 5 mm, this screw is specifically designed for guided bone regeneration (GBR) protocols. Its structure integrates a self-tapping thread that facilitates its anchoring in the maxillary or mandibular bone structures. Manufactured by Jeil Medical Corp., it is distinguished by its silver finish and technical reference 241.011605, offering practitioners a precise solution for the stabilization of graft materials or protective membranes.
What are the clinical indications for this osteosynthesis screw?
This oral surgery titanium screw is primarily indicated for the mechanical stabilization of bone grafts (onlay) and the fixation of non-resorbable or resorbable membranes during ridge augmentation procedures. In implantology and periodontology, it allows for the strict immobilization necessary for the osseointegration of filling materials. Its use is common in cases of complex bone defects requiring volumetric reconstruction before or during implant placement. The choice of the 5 mm length must be adapted to the thickness of the cortical bone and the device to be fixed.
What are the technical characteristics of the 241.011605 screw?
The Jeil Medical titanium self-tapping screw presents rigorous specifications to meet the requirements of micro-surgery. With a diameter of 1.6 mm, it belongs to the category of small-caliber screws, ideal for restricted interdental spaces or areas of low bone volume. Its total length is 5 mm. The self-tapping characteristic means that the tip and thread are designed to cut their own path into the bone, thereby reducing the need for extensive preparation of the recipient site. This technical design ensures optimal primary stability of the surgical assembly upon insertion.
What are the contraindications for the use of this device?
Although specific data are not listed, general contraindications for the use of a 1 6 osteosynthesis screw include uncontrolled systemic pathologies affecting bone metabolism or healing. Insufficient oral hygiene or active infections at the surgical site constitute major contraindications. Furthermore, any known allergy to the constituent metals of the device (generally titanium or its alloys) must preclude its use. It is imperative to consult the technical instructions from the manufacturer Jeil Medical Corp. to identify all clinical situations where the placement of this material is discouraged.
What are the precautions for use for a non-resorbable screw?
The Jeil Medical dental self-tapping screw is a non-resorbable device, meaning it remains stable in the body until its eventual surgical removal. The practitioner must ensure that the screw head does not create areas of irritation for the surrounding soft tissues, which could lead to exposure of the material. Total tension-free mucosal coverage is recommended after placement. The removal of the screw is generally performed after the bone consolidation phase, often during the implant placement phase or site reopening, using the handling instruments adapted to the Jeil Medical range.
Who is the manufacturer and what standards are respected?
The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of maxillofacial and dental osteosynthesis. As a product distributed by Delynov, this screw meets industrial manufacturing standards for implantable medical devices. Although specific certifications (regulatory class or CE marking) are not detailed in the source data, Jeil Medical follows the rigorous quality control protocols specific to micro-osteosynthesis devices. Healthcare professionals are invited to check the regulatory markings present on the sterile packaging before any clinical use to ensure compliance with local requirements.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | JEIL MEDICAL |
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