Barrier Casaque SP PRIM PL L-L (580201-00) Mölnlycke - Delynov

What is the Mölnlycke BARRIER® SP PRIM PL surgical gown?

The BARRIER® SP PRIM PL surgical gown, referenced under code 580203-00 by the manufacturer Mölnlycke, is a personal protective device designed for operating environments. This specific model, offered in size XL-L, belongs to the Primary Plus (PRIM PL) range from Mölnlycke Health Care. This product is packaged in boxes of 32 pieces, providing a logistical solution tailored to the needs of oral surgery and implantology clinics. As an essential element of sterile draping, this gown aims to maintain an effective barrier between the surgical team and the operative field, thereby limiting the risks of cross-contamination during invasive procedures.

What are the clinical indications for this surgical gown?

The use of the Mölnlycke BARRIER® surgical gown is indicated during surgical procedures requiring the maintenance of rigorous asepsis. In dental, oral, and implant surgery, wearing this gown is recommended to protect the practitioner and the assistant against splashes of biological fluids while preserving the sterility of the intervention area. It is perfectly suited for implant placement, sinus lift, or complex periodontal surgery. Its XL-L size design allows for optimal freedom of movement for the surgeon, guaranteeing comfort during long-duration interventions while ensuring adequate body coverage.

What are the technical characteristics of reference 580203-00?

Technical reference 580203-00 corresponds to the BARRIER® SP PRIM PL gown developed by Mölnlycke. This model is distinguished by its ergonomic cut in size XL-L, adapted to the morphology of practitioners requiring a significant range of motion. Although the exact material specifications are not detailed in the source data, the BARRIER® range is recognized for its ability to serve as a protective barrier in clinical settings. The packaging per box of 32 pieces ensures simplified inventory management for healthcare facilities. This device integrates into a strict hygiene protocol, meeting protection requirements during the critical phases of surgery.

What are the contraindications for the use of this device?

There are no specific clinical contraindications mentioned for the use of this surgical gown, other than compliance with standard asepsis protocols. However, it is imperative not to use the product if the individual packaging is damaged or opened before the intervention, as the sterility of the device would no longer be guaranteed. Practitioners must also ensure that the XL-L size is adapted to their morphology to avoid any risk of contamination due to an inappropriate fit. In case of doubt regarding compatibility with certain chemical agents or in case of a known allergy to medical textile components, it is recommended to consult the technical instructions provided by the manufacturer Mölnlycke Health Care.

What are the precautions for use and storage for these gowns?

Mölnlycke BARRIER® gowns are single-use devices. They must under no circumstances be resterilized or reused, as this would compromise the integrity of the protective barrier and increase the risk of healthcare-associated infections. After each oral surgery intervention, the gown must be disposed of according to current protocols for clinical waste with infectious risks (DASRI). For storage, it is advised to keep the box of 32 pieces in a dry place, away from direct light and humidity, in order to preserve the technical properties of the product until its use. Compliance with these instructions guarantees the performance of the device during each surgical act.

Who is the manufacturer and what is the regulatory information?

This device is manufactured by Mölnlycke Health Care, a world leader in the design of surgical and wound management solutions. The Mölnlycke brand is synonymous with quality and reliability in the medical sector. Regarding regulatory aspects such as the device class or specific CE marking, this information is not specified in the current technical documentation. Users are invited to systematically refer to the product labeling and the instructions for use attached to the box of 32 pieces to verify the certifications in force and compliance with European standards relating to protective surgical gowns.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.