DEMO Blouse de protection jaune L (1901-31) Mölnlycke - Delynov (copie)

What is the Mölnlycke green protective gown size L?

The green protective gown size L, referenced under code 1903-31 by the manufacturer Mölnlycke Health Care, is a medical protective garment designed to cover the torso and arms of healthcare professionals. Delivered in boxes of 50 pieces, this gown constitutes a fundamental element of protective attire in dental offices or hospital environments. Its structure is designed to provide a protective barrier against splashes and environmental contaminants, while respecting the quality standards associated with the Mölnlycke brand. This device is specifically sized in size L to adapt to the morphology of practitioners and assistants during daily interventions.

What are the clinical indications for this protective garment?

This surgical protective garment is indicated for all clinical situations requiring the maintenance of rigorous hygiene and the protection of personnel against biological agents. In oral, periodontal, or implant surgery, the use of this green protective gown helps prevent cross-contamination between the patient and the caregiver. It is recommended during the preparation phases of the operating room, during routine dental care generating aerosols, or when handling soiled medical devices. Its use is part of standard protocols for the prevention of healthcare-associated infections, guaranteeing a secure working environment for the entire healthcare team.

What are the technical characteristics of reference 1903-31?

The technical reference 1903-31 from Mölnlycke corresponds to a green protective gown model, offered in size L. This dental protective garment is packaged in boxes of 50 units, which facilitates stock management for facilities with high surgical activity. Although specific material details are not detailed in the raw technical sheet, the design by Mölnlycke Health Care ensures manufacturing oriented towards the needs of the medical sector. The cut is intended not to hinder the freedom of movement of the dental surgeon, a crucial point during precision gestures in implantology or soft tissue surgery. The green color is a visual standard allowing for rapid identification of the type of protection within the practice.

What are the contraindications for the use of this protective gown?

There are no specific documented medical contraindications for wearing this medical protective garment, apart from a possible individual sensitivity to the textile components used by the manufacturer Mölnlycke Health Care. However, it should be noted that this protective gown is not intended to replace sterile operating room attire if the surgical procedure requires a total level of asepsis according to current protocols. The user must ensure that size L is correctly adjusted to avoid any risk of snagging or accidental exposure. In the event of a tear or significant soiling during an intervention, it is imperative to replace the gown immediately to maintain the integrity of the protective barrier.

What are the precautions for use and waste management?

This office protective garment is a single-use device. To guarantee optimal safety, it must under no circumstances be washed, reprocessed, or reused. After each intervention or as soon as the gown is contaminated by biological fluids, it must be removed using a strict aseptic technique to avoid any contact with the skin or undergarments. Once removed, the protective gown must be disposed of in accordance with the protocols for the disposal of clinical waste with a risk of infection (DASRI) in force in the establishment. Compliance with these precautions minimizes the risk of pathogen spread within the dental office and ensures compliance with hospital hygiene rules.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Mölnlycke Health Care, a recognized player in the field of surgical solutions and wound management. The Mölnlycke brand is a guarantee of quality and reliability for healthcare professionals. Regarding specific certifications such as the regulatory class or CE marking, this information is not specified in the current technical data for reference 1903-31. It is therefore recommended that users systematically refer to the product labeling and the instructions for use provided by the manufacturer to verify compliance with the European standards in force at the time of purchase. Delynov is committed to providing products from trusted manufacturers for the safety of care.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.