Name: Meditrade 2403 Superslip® Super Incontinence Brief Medium
Brand: Meditrade
SKU: MDT-2403
Price: 57.64 EUR
Availability: InStock
Rating: 4.7 (7 reviews)

Hygiene Supplies

Meditrade

Meditrade Superslip® Super Incontinence Brief Medium

EN ISO 13485:2003 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance.

EN ISO 13485:2003/AC:2007 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, amended on 2007.

EN ISO 13485:2003/AC:2009 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, amended on 2009.

EN ISO 13485:2012 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, updated from the 2003 version.

EN ISO 13485:2012/AC:2012 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, updated and amended in 2012.

EN ISO 13485:2016 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, updated from the 2012 version.

EN ISO 13485:2016/A11:2021 is a standard for quality management systems for medical devices. It sets guidelines for design and development, production, installation and servicing of medical devices. Test results include measurements of compliance with the standard's requirements. It also includes guidelines for continual improvement, risk management and regulatory compliance. This is a specific version of the standard, updated and amended in 2021.

EN ISO 13485:2016/AC:2016 is a standard that defines the requirements for a quality management system for the design and manufacture of medical devices. It specifies the design and performance requirements for the medical device, the test methods for validation of the product, and the marking and labelling of the product. The standard also includes requirements for management responsibilities, design and development, production, inspection and testing, and post-market surveillance. The test results will show if the product meets the requirements of the standard and is safe for use as a medical device.

EN ISO 13485:2016/AC:2018 is an updated version of the standard EN ISO 13485:2016 which defines the requirements for a quality management system for the design and manufacture of medical devices. It specifies the design and performance requirements for the medical device, the test methods for validation of the product, and the marking and labelling of the product. The standard also includes requirements for management responsibilities, design and development, production, inspection and testing, and post-market surveillance. The test results will show if the product meets the requirements of the standard and is safe for use as a medical device. The 2018 version of the standard includes some technical updates and clarifications to the 2016 version.

Identifies the primary substance composition affecting product performance, durability, safety, and environmental impact in hygiene applications.

The visual appearance that may indicate purpose in color-coded cleaning systems, match facility aesthetics, or help identify product types in various environments.

Indicates how the hygiene garment secures around the body, affecting comfort, fit, and ease of use during daily activities or specialized care.

Offers an adjustable and secure seal. Provides flexibility in tightening/loosening, adapting to varied contents and preventing spills or leaks.

Provides a flexible, conforming, and easily adjustable fit. Ensures a secure and comfortable closure, adapting to various body shapes and movements.

Cleaning & Hygiene Supplies, also known as janitorial supplies or sanitation products, encompass a wide range of items designed to maintain cleanliness and promote health in various environments. This category includes cleaning chemicals, disinfectants, paper products, hand sanitizers, and cleaning equipment such as mops and vacuum cleaners. Key industries that rely on these supplies include healthcare, manufacturing, food processing, hospitality industry, and education. These products are essential for ensuring a safe and sanitary environment, helping to prevent the spread of contaminants and maintain operational efficiency.

Hygiene supplies encompass a range of products designed to maintain cleanliness and promote health in various environments. Commonly referred to as sanitation supplies or janitorial products, these items include hand sanitizers, disinfectants, paper towels, and cleaning agents. Key industries utilizing these supplies include healthcare, food processing, manufacturing, and hospitality, where maintaining high standards of hygiene is critical for safety and compliance.

Incontinence Products, commonly referred to as Adult Diapers or Absorbent Pads, constitute a range of items specially designed to manage and contain urinary or fecal incontinence. They provide comfort, discretion, and protection to users. Key industries utilizing these products predominantly include Healthcare, Elderly Care, and Disability Services where maintaining personal hygiene and dignity of patients or elderly individuals is paramount. The use of such products can also extend into the personal care and hospitality sector. With a discreet design and high absorbency, these products play a critical role in supporting self-care and independent living.

Incontinence Pads offer discreet, reliable protection for light to moderate urinary leakage. These absorbent, comfortable pads feature skin-friendly materials and various absorption levels to suit individual needs, helping users maintain confidence and independence throughout daily activities.

Meditrade GmbH is a reputable brand, renowned for its high-quality gloves and disinfection products. Founded in Germany, this esteemed company has been serving the healthcare and personal protection industries for over three decades. Over the years, Meditrade GmbH has established itself as a market leader, providing reliable solutions for hygiene and safety. Their product range, including durable gloves and effective disinfectants, is a testament to their commitment to quality and efficacy. Trust and credibility are at the heart of the Meditrade GmbH brand, making it a preferred choice for professionals across Europe.

Meditrade Superslip® Super Incontinence Brief Medium

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