Foqus PGCL USP 2.0 Triangular Needle 2.0 mm

Foqus PGCL USP 2.0 Triangular Needle 2.0 mm is a specialist product designed to meet the needs of professionals working in the surgical, veterinary or advanced suturing procedures. The triangular needle associated with a PGCL (Poliglecaprone 25) suture thread guarantees precision, safety and reliable hold during the suturing of soft tissues, promoting effective closure and optimal healing. The 2.0 mm size facilitates precise control during application, reducing the risk of accidental injury while ensuring robustness thanks to the high quality of the materials used. The Foqus PGCL sutures are designed to offer ease of maneuver, very low memory and easy manipulation, minimizing tissue trauma and facilitating management even in the most complex and delicate situations.

The triangular needle provides effective penetration, optimal for passing through fibrous and resistant fabrics, offering a clean and precise cut that limits resistance and the formation of burrs or tears. The specific shape allows for very high suturing precision, maintaining the resistance required for procedures that require maximum reliability. The length and shape of the needle provide excellent visibility and maneuverability, fundamental characteristics especially during demanding interventions and operations in confined spaces.

Choosing the USP 2.0 size ensures an ideal balance between ease of handling and wire strength, resulting in a very versatile solution that is well suited to a wide range of surgical applications. Foqus PGCL USP 2.0 Triangular Needle 2.0 mm was designed to guarantee constant performance, safety for the operator and the patient, as well as excellent compatibility with various surgical instruments and automatic sutures.

Therapeutic Indications

Foqus PGCL USP 2.0 Triangular Needle 2.0 mm is indicated for the suturing of soft tissues where an absorbable suture characterized by maximum insertion precision and reduced tissue trauma is required. It is particularly recommended in cases where a rapid healing phase is required and where initial strength needs must be balanced with a gradual decrease in thread holding force as the tissue heals. The product is widely used in general surgery, in the treatment of surgical and traumatic wounds, in both superficial and deep suturing procedures, especially in the veterinary field, but also in hospital practice on human patients. It is suitable for external and internal sutures, including use in abdominal, gynecological, urological and skin surgery, supporting the healing of cuts, surgical incisions, lacerations and suturing of skin grafts.

The product is also used in suturing procedures where accurate positioning control and high safety are required, such as in the suturing of parenchymatous organs and delicate tissues. Rapid absorption reduces the need for subsequent removal, minimizing post-operative discomfort and the risk of secondary complications associated with permanent sutures. The triangular needle also allows you to easily deal with higher density fabrics, ensuring reliable penetration even in particularly resistant conditions. This makes the product particularly suitable in cases where a resistant but temporary suture is required, destined to dissolve without the need for further interventions.

Triangular needle sutures are also indicated in procedures where it is essential to preserve the integrity of the tissues as much as possible and reduce the risk of inflammation or local reaction, promoting regular and uniform healing. Thanks to its versatility and safety, the Foqus PGCL USP 2.0 Triangular Needle 2.0 mm adapts to multiple clinical scenarios, making it ideal as a primary choice in numerous surgical practices.

Composition

Active ingredient: The suture thread is composed of Poliglecaprone 25 (PGCL), an absorbable synthetic copolymer derived from glycolide and caprolactone, known for its excellent biocompatibility and mechanical properties. This material is characterized by high initial tensile strength, very low memory which facilitates manipulation during suture placement and predictable degradation through hydrolysis in the tissues.

The associated triangular needle is made of the highest quality surgical steel, specifically designed to offer precise and controlled penetration, ideal for passing through tissues while maintaining a stable conformation and preventing unwanted bending during use.

In detail, the combination between PGCL and the specific shape of the needle makes it possible to satisfy the demands for efficiency of both the surgeon and the patient, optimizing absorption times and reducing the risks of complications due to prolonged stay of the suture. No elements of animal origin are used in the composition of the thread and needle, further increasing safety of use even in sensitive subjects.

The needle measures 2.0 mm, perfectly calibrated to provide the best combination of penetration and control, reducing the risk of collateral damage and improving the handling of the device during any type of intervention.

Contraindications

Do not use Foqus PGCL USP 2.0 Triangular Needle 2.0 mm in patients with known hypersensitivity to Poliglecaprone 25 or other similar synthetic polymers, nor in subjects with severe allergic reactions to surgical steels or their alloys used in needles. The product must not be used in the suturing of cardiovascular or neurological tissues, nor in areas where the presence of persistent infections or abundant secretions which could negatively interfere with the natural absorption process of the material is likely.

Avoid its use in immunocompromised patients or with conditions that delay tissue healing, as complications may occur due to the more rapid absorption of the suture thread compared to the natural healing process. The Foqus PGCL Suture is not designed for situations where long-lasting mechanical strength beyond that provided by the intended period of tissue support is required, such as in high-stress repairs or in areas subject to intense and prolonged motion.

The use in pediatrics or in patients with specific pathologies should be evaluated on a case-by-case basis by the responsible doctor, taking into account the individual characteristics and clinical history of the subject. Do not use if the package is damaged, if the thread or needle shows signs of deterioration, contamination or improper handling.

Safety of the drug for the species

Foqus PGCL USP 2.0 Triangular Needle 2.0 mm has been developed to ensure maximum safety for both the operator and the patient. The biocompatibility of PGCL material is widely recognized, thanks to its hypoallergenic properties and the absence of potentially harmful residues during product degradation. In the tissues, the suture maintains an optimal safety profile, degrading in a controlled manner without releasing toxic substances, minimizing local inflammatory reactions and promoting wound healing.

The triangular needle, thanks to its robust but flexible structure, allows safe handling, reducing the risk of accidental injury to both the surgeon and the treated tissues. The use of excellent materials prevents the risk of accidental breakages or corrosion even during long-lasting procedures, helping to maintain the performance of the product unaltered until the completion of the intervention.

Laboratory tests, together with clinical observations, confirm the total absence of significant side effects related to the use of the product in the indicated species. In rare cases, mild local reactions such as redness or edema may occur which generally resolve spontaneously without the need for further treatment.

The safety of the suture is further strengthened by the speed and predictability of absorption, avoiding accumulations of material or possible foreign body effects in the tissues. The absence of elements of animal origin also prevents any risk of transmission of zoonotic diseases or prions.

Precautions

When using the Foqus PGCL USP 2.0 Triangular Needle 2.0 mm some fundamental precautions must be taken to ensure the highest level of safety and optimal results. The operation must be conducted by qualified personnel experienced in the use of triangular needles and absorbable synthetic threads, strictly respecting correct asepsis practices and standard surgical procedures. Before use, it is essential to check the integrity of the packaging and the sterility of the product. Do not use if the device appears to have been tampered with or contaminated. After opening, use immediately to avoid the risk of environmental contamination.

Handle the needle carefully to prevent accidental injuries and dispose of sharp instruments in compliance with specific safety regulations. Avoid any recycling or reuse of the product once removed from the packaging, do not attempt to straighten or correct any deformities of the needle, as this could compromise the safety of the procedure. The duration and absorption methods of the thread may vary based on the individual conditions of the fabrics; in case of infections or presence of alterations, carefully monitor the treated area and evaluate the possible need for additional interventions.

Wash your hands carefully after the procedure and do not allow inexperienced people or people without suitable health protection to handle the product. Pay particular attention in situations with high risk of infection, in debilitated or immunocompromised patients.

Method of administration

The application of Foqus PGCL USP 2.0 Triangular Needle 2.0 mm must follow a specific protocol that guarantees maximum effectiveness in closing the wound and reducing the risk of complications. After preparing the operating field in completely sterile conditions, select the length of the thread and the shape of the needle based on the type of tissue to be sutured and the depth of the wound. The triangular needle must be held firmly and inserted delicately, following an angle that minimizes resistance and tissue trauma. Proceed with regular and constant steps, avoiding excessive tension which could compromise the tightness of the suture or damage the edges of the wound.

Once the suture is finished, knot the thread using a technique suitable for the specific clinical situation, preferably applying multiple knots to ensure a firm fixation. Cut the excess thread and check the correct closure of the flaps, making sure that there are no areas of anomalous tension or areas of necrosis. Monitor the area over the next few days for signs of inflammation, allergic reaction, or failure of the thread to hold. If necessary, consult the specific clinical protocol or request specialist assistance.

Treatment program

The treatment program with Foqus PGCL USP 2.0 Triangular Needle 2.0 mm varies depending on the type of wound and the tissue affected. In general, the suture must be applied immediately after cleaning and preparing the operating field, proceeding according to the pattern most suited to the type of wound: simple interrupted stitches, continuous sutures, mattresses or other specialized techniques. The duration of support provided by PGCL thread is generally between 2 and 4 weeks, with a progressive loss of resistance in the later phase accompanying tissue healing.

Complete reabsorption occurs within approximately 90-120 days, without the need for removal. In particular cases, especially in the presence of large lesions or infections, the doctor may consider integrating the therapy with additional sutures or topical remedies. Post-operative monitoring is essential: periodically check the area to early identify any signs of dehiscence, infection or adverse reaction.

In the presence of complications or in case of delayed healing, it is advisable to plan specific follow-ups with objective examinations and periodic evaluations of the tightness of the thread, to guarantee the complete and safe resolution of the healing process.

Target species

Foqus PGCL USP 2.0 Triangular Needle 2.0 mm is mainly intended for the suturing of soft tissues in both the veterinary and human fields. It is suitable for use on dogs, cats and other animal species where the absorbable suture is advantageous compared to permanent solutions, allowing optimal management of the healing process without the need for subsequent thread removal operations. In the human field it is indicated for a wide range of surgical specialties thanks to its high safety and effectiveness. The adaptability of the product allows it to be used in different types of procedures, where the balance between temporary resistance of the suture and controlled absorption represents an indispensable characteristic for the success of the operation.