Ivory Matrix Medium Molar 0.05mm - 12 pieces 4979/2 - Medesy (4979/2)
The Matrice ivoire molaires medium 0,05mm - 12 pièces 4979/2 - Medesy (4979/2) is a medical device manufactured by Medesy S.r.l..
- Manufacturer: Medesy S.r.l..
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the ivory molar matrix medium 0.05mm - 12 pieces 4979/2 - Medesy?
The ivory molar matrix medium 0.05mm is a thin metallic device designed by Medesy for restorative dentistry. This product, referenced under code 4979/2, comes in the form of a 0.05mm thick band specifically sized for medium-sized molars. Packaged in a set of 12 pieces, this ivory dental matrix is an essential consumable for delimiting the walls of the tooth during the placement of filling materials. It compensates for the absence of a natural wall and guides the practitioner in reconstructing the dental morphology, thus ensuring appropriate sealing and anatomical shape at the proximal surfaces of the molars.
What are the clinical indications for this molar dental matrix?
The use of the molar matrix 0 05 is indicated for performing Class II direct restorations on molars. In conservative dental surgery, it is used to isolate the treated tooth from adjacent teeth and to contain the restorative material (composite, amalgam, or cement) within the prepared cavity. The molar ivory matrix is particularly useful for restoring the interproximal contact point, thereby preventing post-operative food impaction and gingival inflammation. It adapts to the contours of the medium molar to provide a rigid and stable temporary framework during the polymerization or setting phase of the filling material.
What are the technical characteristics of this Medesy product?
The ivory matrix 0 05mm features precise technical specifications to meet the requirements of restorative care. Its 0.05mm thinness is a major asset, allowing easy passage into interdental spaces even when contact points are tight, while maintaining sufficient mechanical strength not to deform under condensation pressure. This model 4979/2 from Medesy is calibrated for medium-sized (medium) molars. The metallic design ensures compatibility with various Ivory-type matrix holder systems, guaranteeing rapid placement and secure removal after the restoration has hardened without altering the surface finish of the material.
What are the contraindications for the use of the ivory matrix 0 05mm?
Although no specific medical contraindications are listed in the source data for this consumable, the use of the molar ivory matrix must be evaluated by the practitioner based on the patient's clinical condition. Generally, the use of metallic matrices may be contraindicated in patients with a known hypersensitivity to metals if the composition includes allergenic alloys. Clinically, it should not be used if the integrity of the marginal gingiva does not allow for stable placement or if the coronal destruction is too extensive to allow for anchoring of the matrix holder. Reference should systematically be made to the technical instructions from the manufacturer Medesy S.r.l. for detailed precautions for use.
What are the precautions for use for these non-resorbable matrices?
As it is a non-resorbable device, the ivory dental matrix must be imperatively removed once the restorative material has stabilized. The practitioner must ensure that no metallic fragments remain in the gingival sulcus after the procedure. During placement, particular attention must be paid to the cervical adjustment to avoid material overhangs that could damage the periodontium. Although sterility specifications are not detailed here, this type of consumable must be handled according to the hygiene protocols in force at the dental practice. Removal must be performed with care, often using pliers, so as not to fracture the freshly completed restoration.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Medesy S.r.l., a company recognized for manufacturing instruments and consumables for dental surgery. Regarding regulatory standards such as the medical device class or specific CE marking, this information is not specified in the current technical data of the product sheet. However, as an established European manufacturer, Medesy designs its products according to professional quality standards. For any information relating to MDR compliance or ISO certifications specific to reference 4979/2, it is recommended to consult the official technical documentation provided by the manufacturer or contact Delynov support services.
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