Ethicon Johnson - NW9262 - PDS*II Suture USP 1-0 NW 9262 Taperpoint, 12 Foils Box

This product is a sterile, synthetic, absorbable monofilament suture designed for use in surgical procedures. The suture material is polydioxanone polymer, a synthetic absorbable polymer. It is colored violet to enhance visibility during surgical manipulation.

The suture exhibits a predictable absorption profile, with significant tensile strength retention over a period of several weeks. Specifically, it retains approximately 70% of its initial tensile strength at two weeks post-implantation, 50% at four weeks, and 25% at six weeks. The complete absorption of the suture material by hydrolysis occurs between 180 and 210 days.

This suture is supplied with a needle, identified as a 1/2 circle round body heavy needle, measuring 48mm in length. The suture itself has a length of 150 cm and is classified as USP 1-0 in diameter. Each unit contains 12 individually foil-sealed packages of the suture and needle combination.

The sterile nature of the product is maintained through its packaging, ensuring its suitability for surgical environments. The polydioxanone material offers a smooth passage through tissue, minimizing drag and trauma during suturing. Its absorbable nature eliminates the need for suture removal in many applications, contributing to patient comfort and reducing the risk of complications associated with retained foreign bodies.

The consistent tensile strength profile makes it suitable for procedures requiring prolonged wound support during the critical healing phases. The violet coloration aids in clear visualization against the backdrop of surgical tissues, facilitating precise placement and knot tying. The combination of a robust needle and a pliable, yet strong, suture thread allows for secure tissue approximation.

The product is intended for single use, and proper handling and sterilization protocols should be followed prior to use to maintain its sterility. The packaging is designed to protect the integrity of the suture and needle until the point of use. The material composition and manufacturing process adhere to established medical device standards.

The specific needle geometry and size are chosen to complement the suture's characteristics for optimal performance in various surgical settings. The product is supplied in a box containing 12 individual foil-sealed units. The USP classification indicates the suture's diameter according to United States Pharmacopeia standards.

The monofilament construction minimizes the potential for bacterial harboring, which can be a concern with multifilament sutures. The predictable degradation rate of polydioxanone is a key factor in its selection for specific surgical applications where sustained wound support is required during the initial stages of healing. The suture is designed to be biocompatible and to elicit a minimal tissue reaction.

The tensile strength retention data provides a quantitative measure of its mechanical integrity over time, allowing surgeons to select the appropriate suture for the duration of wound support needed. The product is intended for use by trained medical professionals in a sterile surgical field. The packaging clearly indicates the suture size, needle type, and lot number for traceability.

The product is supplied in a box containing 12 units, each individually packaged for sterility.