Gloves are designed to safeguard hands from various hazards in industrial environments. They are commonly used to protect against chemicals, abrasions, cuts, and extreme temperatures. Key industries that rely on gloves include manufacturing, construction, healthcare, and food processing. These gloves come in various materials such as latex, nitrile, and leather, each offering specific benefits like chemical resistance, durability, and dexterity. By selecting the appropriate type of glove, businesses can enhance worker safety and maintain compliance with industry standards.

Packaging Supplies, also known as packing materials or shipping supplies, encompass a wide range of products designed to protect, contain, and transport goods efficiently. These supplies include items such as boxes, bubble wrap, packing peanuts, tape, and pallets. Key industries that rely heavily on packaging supplies include manufacturing, logistics, e-commerce, food and beverage, pharmaceuticals, and retail. These materials are essential for ensuring product safety, reducing damage during transit, and optimizing storage and handling processes.

Safety Equipment, also known as Personal Protective Equipment (PPE), encompasses a range of products designed to protect workers from hazards in the workplace. This category includes items such as helmets, gloves, goggles, hearing protection, and respiratory masks. Key industries that rely heavily on safety equipment include construction, manufacturing, oil and gas, mining, and chemical processing. These products are essential for ensuring worker safety and compliance with industry regulations.

Workwear, also known as industrial clothing or protective apparel, encompasses a range of garments designed to ensure safety, durability, and comfort for workers in demanding environments. Commonly used in industries such as construction, manufacturing, oil and gas, and utilities, workwear includes items like coveralls, high-visibility vests, flame-resistant clothing, and safety footwear. These products are essential for protecting workers from hazards, enhancing visibility, and maintaining compliance with safety regulations.

Food Service & Restaurant Supplies encompass a wide range of products essential for the efficient operation of food establishments. This category, also known as commercial kitchen supplies or foodservice equipment, includes items such as cookware, utensils, and storage solutions. Key industries that rely on these supplies include restaurants, catering services, hotels, and institutional food service providers such as schools and hospitals. These products are crucial for maintaining high standards of food safety, hygiene, and operational efficiency.

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.

Tools, Tapes & Bolts encompass a wide range of essential items used for construction, maintenance, and repair tasks across various industries. This category includes hand tools, power tools, adhesive tapes, and fasteners such as bolts, screws, and nuts. Commonly referred to as hardware supplies or fastening solutions, these products are indispensable in sectors like manufacturing, construction, automotive, and aerospace. They ensure the structural integrity and functionality of machinery, buildings, and vehicles, making them critical for procurement buyers focused on quality and reliability.

Meditrade Alcoman disinfectant in 18 bottles. 500ml per bottle. Hygienic and surgical hand disinfection. Not suitable for disinfection of open wounds. Dermatologically tested. Highly flammable. Keep away from sources of ignition. Alcoman does not kill spores and is therefore not suitable for sterile instruments and syringes. See instructions for use for more information.

Meditrade Alcoman disinfectant in 2 canisters. 5l per canister. Hygienic and surgical hand disinfection. Not suitable for disinfection of open wounds. Dermatologically tested. Highly flammable. Keep away from sources of ignition. Alcoman does not kill spores and is therefore not suitable for sterile instruments and syringes. See instructions for use for more information.

Meditrade Vinyl 2000 PF Examination glove made of vinyl, powder-free

Meditrade Nitril® Black examination glove made of nitrile, powder-free

Meditrade Nitril® NextGen® Examination glove made of nitrile, powder-free

Meditrade Alcoman®+ Hand disinfection, 1 L

Soap/disinfectant dispenser for disposable bottles and refills. Aluminium housing and short operating lever. Suitable for 500 ml or 1000 ml containers. Suitable for wall mounting. Model with reusable pump or one-way pump, interchangeable at the front.

Meditrade Gentle Skin Superior OP™ Glove made of latex, powder free

Meditrade Bed cover hood, HT, 320 cm x 95 cm

Meditrade Nitril® 3000 Nitrile examination glove, powder-free

Dermatologically Tested refers to products that have been tested and proven to be safe for use on the skin. The European Union has regulations for cosmetics products, which includes dermatological testing, to ensure that products are safe for use. To be labeled as dermatologically tested, the product must be tested by a qualified professional, such as a dermatologist, and must not cause any irritation or allergic reactions. The testing must be carried out on a representative sample of human volunteers and the results must be evaluated by a qualified professional before the product can be considered as dermatologically tested and can bear the label. The EU Cosmetics Regulation, lays out the specific requirements for safety assessments and labeling of cosmetics products.

EN 14476:2005+A1:2006 is a European standard that sets the rules for chimneys made of clay. The standard explains how the chimneys should be made, how strong and durable they must be, and how they should be tested to make sure they meet these rules. The amendment A1:2006 includes additional requirements for the performance of chimneys and additional test methods to check the performance of the chimneys. Possible test results include measurements of strength, stretchiness, and how well the chimneys resist fire. The standard helps make sure chimneys made of clay are safe to use.

EN 14476:2013 – prA2:2016 is a European standard that sets the rules for chimneys made of clay. The standard explains how the chimneys should be made, how strong and durable they must be, and how they should be tested to make sure they meet these rules. The proposal for amendment A2:2016 contains proposed changes, additions or corrections to the original standard EN 14476:2013 . Possible test results include measurements of strength, stretchiness, and how well the chimneys resist fire. The standard helps make sure chimneys made of clay are safe to use.

EN 14476:2005 is a European standard that sets the rules for chimneys made of clay. The standard explains how the chimneys should be made, how strong and durable they must be, and how they should be tested to make sure they meet these rules. Possible test results include measurements of strength, stretchiness, and how well the chimneys resist fire. The standard helps make sure chimneys made of clay are safe to use.

EN 14476:2013+A1:2015 is a European standard for testing the effectiveness of disinfectants and sterilants against the virus that causes COVID-19. It defines test methods, performance requirements, and possible test results. The standard requires a minimum log reduction (inactivation) of 4.0 (99.99%) for virucidal claim. Testing must be done using a suspension of a reference virus and the product must be tested according to the manufacturers' instructions for use. The +A1:2015 is an amendment to the original standard, which provides additional information and guidance on testing.

EN 14476:2013+A2:2019 is a European standard for testing the effectiveness of disinfectants and sterilants against the virus that causes COVID-19. It defines test methods, performance requirements, and possible test results. The standard requires a minimum log reduction (inactivation) of 4.0 (99.99%) for virucidal claim. Testing must be done using a suspension of a reference virus and the product must be tested according to the manufacturers' instructions for use. The +A2:2019 is an amendment to the original standard, which provides additional information and guidance on testing and also includes new requirements for testing virucidal activity against other enveloped viruses.

EN 14476:2013 is a European standard for testing the effectiveness of disinfectants and sterilants against the virus that causes COVID-19. It specifies the test methods, performance requirements, and possible test results for determining a product's virucidal activity. The standard requires a minimum log reduction (inactivation) of 4.0 (99.99%) for virucidal claim. Testing must be done using a suspension of a reference virus and the product must be tested according to the manufacturers' instructions for use.

EN 12791:2005 is a European standard for determining the virucidal activity of chemical disinfectants and antiseptics used in medical areas. It specifies a test method for determining the virucidal activity of a chemical disinfectant or antiseptic against a reference test virus (HIV-1, BVDV, Hepatitis B virus, Hepatitis C virus) within a 15 minutes of exposure to the disinfectant or antiseptic. The test requires a minimum of a 4 log10 reduction in the number of virus and the test results should be reported as a quantitative value. The disinfectant or antiseptic must pass the test in order to be certified as meeting the standard.

EN 12791:2016+A1:2017 is a European standard for determining the virucidal activity of chemical disinfectants and antiseptics used in medical areas. It specifies a test method for determining the virucidal activity of a chemical disinfectant or antiseptic against a reference test virus (HIV-1, BVDV, Hepatitis B virus, Hepatitis C virus) within a 15 minutes of exposure to the disinfectant or antiseptic. The test requires a minimum of a 4 log10 reduction in the number of virus and the test results should be reported as a quantitative value. The disinfectant or antiseptic must pass the test in order to be certified as meeting the standard. A1:2017 is an amendment to the EN 12791:2016 standard, which means it makes small changes or corrections to the original standard.

EN 12791:2016 is a European standard for determining the virucidal activity of chemical disinfectants and antiseptics used in medical areas. It specifies a test method for determining the virucidal activity of a chemical disinfectant or antiseptic against a reference test virus (HIV-1, BVDV, Hepatitis B virus, Hepatitis C virus) within a 15 minutes of exposure to the disinfectant or antiseptic. The test requires a minimum of a 4 log10 reduction in the number of virus and the test results should be reported as a quantitative value. The disinfectant or antiseptic must pass the test in order to be certified as meeting the standard. The 2016 version of the standard updates the 2005 version, which means it could have some changes to the original standard.

EN 1500:2013 is a European Standard that specifies the requirements and test methods for the performance of hand sanitizers. It is a revision of EN 1500:1997. The standard defines the minimum requirements for hand sanitizers, including the type of alcohol used (ethanol or isopropanol), the minimum alcohol content, and the test methods for evaluating the effectiveness of the product in killing microorganisms. The performance requirement include the ability to kill certain percentage of germs within a specified time frame and test methods include microbe suspension, and measurement of reduction in the number of microorganisms. The standard also includes a test for hand rubs that uses non-alcohol based products.

EN 1500:1997 is a European Standard that specifies the requirements and test methods for the performance of hand sanitizers. The standard defines the minimum requirements for hand sanitizers, including the type of alcohol used (ethanol or isopropanol), the minimum alcohol content, and the test methods for evaluating the effectiveness of the product in killing microorganisms. The performance requirement include the ability to kill certain percentage of germs within a specified time frame and test methods include microbe suspension, and measurement of reduction in the number of microorganisms.

MD stands for "Medical Device." It refers to any instruments, apparatus, machines, implants, or other similar or related articles that are intended to be used for human beings for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease, injury or disability. In Europe, a MD Label is a special label that must be on all Medical Devices that are sold or used in the European Union (EU). The label must include information about the product, such as the name of the manufacturer, the intended use of the product and CE mark. To be able to sell or use a Medical Device in the EU, the device must meet certain standards and requirements set by the European Union and notified body.

EN 455-3:2015 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2006 version.

EN 455-3:2006 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, and freedom from protein. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, and freedom from protein. This version of the standard includes some changes and updates from the 1999 version.

EN 455-3:1999 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes and freedom from powder. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes and freedom from powder.

EN 455-2:2009+A2:2013 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. This version of the standard includes some changes and updates from the 2009 version.

EN 455-2:2015 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. This version of the standard includes some changes and updates from the 2009 version.

EN 455-2:1995 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, and packaging. Test results can include measurements of the gloves' physical properties, dimensions, and packaging.

EN 455-2:1995/A1:1998 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging and freedom from holes. Test results can include measurements of the gloves' physical properties, dimensions, packaging and freedom from holes. This version of the standard includes some changes and updates from the 1995 version.

EN 455-2:1995/AC:1996 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging and freedom from holes. Test results can include measurements of the gloves' physical properties, dimensions, packaging and freedom from holes. This version of the standard is a Corrigendum version that means that it has minor corrections from the original 1995 version.

EN 455-2:2000 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging and freedom from holes, and also includes requirement for freedom from powder. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes and freedom from powder. This version of the standard includes some changes and updates from the 1995 version.

EN 455-2:2009 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder and freedom from protein. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder and freedom from protein. This version of the standard includes some changes and updates from the 2000 version.

EN 455-2:2009+A1:2011 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein and freedom from endotoxins. Test results can include measurements of the gloves' physical properties, dimensions, packaging, freedom from holes, freedom from powder, freedom from protein and freedom from endotoxins. This version of the standard includes some changes and updates from the 2009 version.

EN 455-1:2020+A1:2022/prA2 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2020 version, and the prA2 version is a provisional version of the standard, that means that is a version that is being reviewed and updated before the final version is published.

EN 455-1:1993/A1:1998 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, and freedom from powder. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging and powder. This version of the standard includes some changes and updates from the 1993 version.

EN 455-1:1993 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, and packaging. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation and packaging.

EN 455-1:2000 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, freedom from powder and freedom from protein. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging, freedom from powder and freedom from protein. This version of the standard includes some changes and updates from the 1993 version.

EN 455-1:2020+A1:2022 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2020 version.

EN 455-1:2020 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins, and freedom from pyrogens. Test results can include measurements of the gloves' freedom from holes, tensile strength, elongation, packaging, freedom from powder, freedom from protein, freedom from endotoxins and freedom from pyrogens. This version of the standard includes some changes and updates from the 2000 version.

EN 455-4:2009 is a European standard for disposable medical gloves. It sets out the definition, performance requirements and test methods for this type of gloves. The standard includes requirements for freedom from holes, dimensions, packaging, freedom from powder, freedom from protein and freedom from endotoxins. Test results can include measurements of the gloves' freedom from holes, dimensions, packaging, freedom from powder, freedom from protein and freedom from endotoxins.

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.

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