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Mini Self Tapping Locking Gold OD - 2.0 L - 8 - JEIL Medical

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The Mini Self Tapping Locking Gold OD - 2.0 L - 8 - JEIL Medical is a medical device manufactured by Jeil Medical Corp..

  • Manufacturer: Jeil Medical Corp..
  • Reference: 241.032008.
  • Reserved for healthcare professionals. Read instructions carefully before use.

36.47 € 36.47 EUR 36.47 € Tax Included 49.96 €

36.47 € Tax Included 49.96 €

(0.00 € / Units)
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GBR

What is the Mini Self Tapping Locking Gold OD - 2.0 L - 8 - JEIL Medical screw?

The Mini Self Tapping Locking Gold OD is a bone fixation device developed by Jeil Medical. It is a technical screw designed for guided bone regeneration (GBR) interventions. This specific model features a length of 8 mm and a diameter of 2.0 mm. Its structure is distinguished by a gold-colored head (Gold) and a locking mechanism (Locking), ensuring a stable interface between the screw and the support. As a fixation component, it plays a crucial role in maintaining graft structures or barrier membranes during the initial bone healing phase.

What are the clinical indications for this Jeil Medical device?

This block or membrane fixation screw is indicated in oral, periodontal, and implant surgery protocols requiring rigid immobilization of graft materials. It is particularly suitable for cases of guided bone regeneration where the stability of the grafted volume is decisive for osseointegration. Practitioners use this type of hardware to fix autogenous or allogenic bone blocks, as well as to secure non-resorbable or resorbable membranes. Its self-tapping function allows for precise application in different bone densities encountered in the maxillae.

What are the technical specifications of reference 241.032008?

The technical reference 241.032008 corresponds to a screw with a diameter of 2.0 mm and a length of 8 mm. The 'Self Tapping' characteristic means that the screw has a thread capable of tapping its own path during insertion, thus reducing the need for complete prior tapping in the bone. The 'Locking' mention indicates a locking system that prevents accidental unscrewing and strengthens the stability of the assembly. The 'Gold' finish allows for quick visual identification during the surgical procedure. This device is designed by Jeil Medical Corp to meet the precision requirements of surgeons specialized in implantology.

What are the contraindications for the use of this fixation screw?

Although specific data are not detailed here, general contraindications for bone fixation devices include uncontrolled systemic pathologies affecting bone metabolism, such as severe osteoporosis or unbalanced diabetes. Use is discouraged in the presence of an active infection at the surgical site or in patients with a known hypersensitivity to metals used in surgical alloys (often titanium-based for this type of material). It is the surgeon's responsibility to evaluate the residual bone quality to ensure that the anchoring of the bone fixation screw is mechanically viable.

What precautions should be taken for this non-resorbable device?

As a metallic fixation device, this screw is by nature non-resorbable. It is intended to maintain mechanical stability for the duration necessary for bone consolidation. Depending on the clinical protocol chosen by the practitioner, the screw may require removal during a second surgical stage (for example, during implant placement or the removal of a non-resorbable membrane). Precautions include controlled tightening to avoid any fracture of the screw neck or excessive compression of the surrounding bone, which could compromise vascularization and tissue regeneration.

Who is the manufacturer Jeil Medical and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., a recognized company in the medical device sector for osteosynthesis and maxillofacial surgery. Although the exact regulatory class and specific CE marking are not mentioned in the current source documentation, Jeil Medical produces its devices according to rigorous quality standards specific to surgical implants. For any precise information regarding certificates of conformity, CE marking, or sterilization instructions, healthcare professionals must imperatively refer to the instructions for use and labeling provided by the manufacturer with product 241.032008.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer JEIL MEDICAL
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GBR