X24 SERAPID incolore 2 (3/0) 1x0.70 DS-18 - Serag Wiessner - Fil de suture

What is the SERAPID absorbable colorless suture (3/0)?

SERAPID is an absorbable surgical suture device developed by Serag-Wiessner. This specific model features a 3/0 (USP) calibre and a structure designed for procedures requiring natural resorption by the body. The thread is supplied in a colorless version to ensure maximum aesthetic discretion during tissue healing. Packaged in boxes of 24 units under reference 3O203214, this material is specifically adapted to the needs of oral and implant surgery, offering a thread length of 70cm for optimal handling ease when tying knots.

What are the clinical indications for this suture in surgery?

This 3/0 calibre SERAPID suture is primarily indicated for the approximation of mucosal edges in oral, periodontal, and implant surgery. Its absorbable structure makes it particularly useful for procedures where suture removal is not desired or is difficult to access. It is perfectly suited for stabilizing flaps after implant placement, tooth extraction, or guided bone regeneration surgery. The needle size and thread strength allow for maintaining adequate tissue tension during the critical phase of primary healing.

What are the technical characteristics of the DS-18 needle?

The DS-18 needle equipped on this Serag-Wiessner suture possesses specific technical properties for dense tissues. The 'DS' code means it is a 3/8 circle needle featuring a triangular reverse cutting tip. This geometry is ideal for passing through gingival tissues without risk of tearing, as the cutting edge is located on the outer curvature. The number '18' indicates a needle body length of 18 mm, offering an effective compromise between maneuverability in the restricted spaces of the oral cavity and the ability to grasp sufficient tissue volumes.

What are the contraindications for the use of SERAPID?

Although specific manufacturer data is not detailed here, general contraindications for absorbable sutures include use on tissues requiring prolonged or permanent mechanical support. SERAPID should not be used in patients with known sensitivities or allergies to the composition materials of synthetic absorbable sutures. It is discouraged to use this type of device in clinical situations where severe infection could compromise the normal resorption process. The practitioner must systematically refer to the Serag-Wiessner manufacturer's technical instructions before any use.

How does resorption occur and what are the precautions?

As the SERAPID suture is absorbable, it is designed to be gradually degraded by the body, generally through a process of hydrolysis. This mechanism spares the patient the sometimes uncomfortable step of suture removal. During handling, it is advised to ensure the precision of the knots to ensure stable hold despite the humidity of the oral environment. The duration of tensile strength and the total resorption time depend on the intrinsic characteristics of the material. It is recommended to clinically monitor the surgical site to ensure that the resorption rate is in line with the patient's own tissue healing kinetics.

Who is the manufacturer and what standards are respected?

This medical device is manufactured by Serag-Wiessner GmbH & Co. KG, a recognized manufacturer in the field of surgical sutures. As a product intended for the European market, it is designed according to rigorous quality standards. Although the precise regulatory class and CE marking are not explicitly mentioned in the current technical source data, Serag-Wiessner products are developed to meet the safety and performance requirements in force for medical devices. For any information regarding specific ISO certifications or MDR compliance, practitioners are invited to consult the official documentation attached to the box of 24 sutures.

State of the art

Modern synthetic sutures - absorbable or non-absorbable - are central to wound healing in oral surgery. Recent advances focus on reducing post-operative infections.