MediInn Latex White Grip disposable latex glove in a pack of 100 pieces.

Very flexible and comfortable latex glove suitable for use in healthcare, food handling and other personal protection.

Medi-Inn Vinyl Comfort is a disposable, non-detergent vinyl patch in a pack of 100 pieces. Suitable for a wide range of general, nursing, healthcare and non-fat food applications.

Medi-Inn disposable nitrile glove in a pack of 200. Soft and durable thin protective glove. Thinner than usual nitrile gloves are suitable for use in healthcare, food processing and other personal protection.

MediInn disposable black nitrile glove in a pack of 100 pieces.

Powder-free and durable protective glove. Black nitrile gloves are suitable for use in beauty care, food processing and other personal protection.

MediInn White Soft disposable, white nitrile glove in a pack of 100 pieces.

Soft and durable thin protective glove. Thinner nitrile gloves are suitable for use in healthcare, food processing and other personal protection.

Medi-Inn disposable 30 cm nitrile glove in a pack of 100.

 Powder-free longer and thicker protective glove. Strong nitrile gloves are suitable for use in healthcare, food processing and other personal protection applications.

MediInn arc hammer in a pack of 300 pieces.

Grey disposable arc honeysuckle. Ester steel.  Length 25,5 cm, width 15 cm, height 4,8 cm. Capacity 700 ml.

Medi-Inn normal shoe covers in a pack of 100 pieces. Blue shoe covers made of CPE material. Suitable for sizes 38-47. Shoe protector with embossed surface, equipped with elastic band.

Medi-Inn disposable wet wipes in packs of 80. The moist wipes are made of non-woven fibres and are intended to be used for skin cleansing. Packed in a dispenser. The wipes can be removed individually. The re-sealable packaging prevents the wipes from drying out and ensures a long shelf life. PH-Neutral. Paraben-free.

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.

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.

ISO 13485:2016 is a standard that specifies requirements for a quality management system for the design and manufacture of medical devices. It includes requirements for how companies should design, implement, maintain and improve their quality management system to ensure that their medical devices are safe and effective. Test results can include information on how well the quality management system is functioning, how well it is being followed, and how effective it is in preventing defects. The standard also includes requirements for how the company should document and record their quality management system performance and continuously improve it.

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 455-2:2009+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 455-2:2009 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 455-2:2000 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 455-2:1995/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 455-2:1995/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 455-2:2015 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 455-2:2009+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 ISO 9001:2015 is a standard that sets out the requirements for a quality management system (QMS). It is a set of guidelines that organizations can follow to ensure that they meet customer requirements and enhance customer satisfaction. The standard is based on the plan-do-check-act model and focuses on continuous improvement. It covers the design, development, production, installation, and servicing of products. Organizations can get certified to this standard, which means that they have been independently audited and found to meet the requirements of the standard. The certification process includes regular audits to ensure that the organization continues to meet the standard's requirements.

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 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 455-1:2020+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+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 ISO 374-5:2016 is a standard that sets rules for testing gloves against chemicals. The standard outlines the performance requirements for gloves to protect against specific chemicals. The test results will show if the gloves meet these requirements or not. Possible test results include information on the gloves' resistance against different chemicals and the duration of protection.

EN 374-5:2016 is a European standard for gloves that protect against microorganisms, specifically gloves that are used for medical and dental procedures. It sets rules for how the gloves should protect against microorganisms and how to test if they meet the standards. Gloves that pass the tests can have a label that says they meet the standard. The test results can be pass or fail for each test that checks the gloves resistance to microorganisms.

EN 420:2003 is a European standard that specifies general requirements for protective gloves. It sets rules for the design, construction, and testing of gloves to ensure they are safe for the user and others nearby. Testing includes measurements of mechanical properties, such as abrasion resistance, cut resistance and tear resistance, as well as for harmful substances, such as phthalates. The standard also includes requirements for labeling and instructions for use. It's an updated version of EN 420:1994 and it's intended to ensure that the gloves provide appropriate level of protection, comfort, and ergonomics and to help the users to choose suitable gloves for their specific application.

EN 420:2003/AC:2006 is a European standard that specifies general requirements for protective gloves. It is an amendment version of the standard EN 420:2003, it includes any modifications or corrections that have been made to the original standard. It sets rules for the design, construction, and testing of gloves to ensure they are safe for the user and others nearby. Testing includes measurements of mechanical properties, such as abrasion resistance, cut resistance and tear resistance, as well as for harmful substances, such as phthalates. The standard also includes requirements for labeling and instructions for use. It's intended to ensure that the gloves provide appropriate level of protection, comfort, and ergonomics and to help the users to choose suitable gloves for their specific application.

EN 420:1994 is a European standard that specifies general requirements for protective gloves. It sets rules for the design, construction, and testing of gloves to ensure they are safe for the user and others nearby. Testing includes measurements of mechanical properties, such as abrasion resistance, cut resistance and tear resistance, as well as for harmful substances, such as phthalates. The standard also includes requirements for labeling and instructions for use. It's intended to ensure that the gloves provide appropriate level of protection, comfort, and ergonomics and to help the users to choose suitable gloves for their specific application.

EN 420:2003+A1:2009 is a European standard that sets out the general requirements for hand protection, including comfort, fit, and dexterity. Performance requirements include resistance to abrasion, cut, tear, puncture, and impact. Test results should show the gloves meet these requirements.

EN ISO 374-4:2019 is a standard that sets the rules for gloves that protect against dangerous chemicals and microorganisms. It tells how gloves should be made, what materials should be used, and how they should be tested. Possible test results include how well the gloves keep out chemicals, how long they last and how well they protect the hands. This standard focus on the use of gloves against specific microorganisms and chemicals, and specifies the performance requirements and test methods for gloves protecting against viral penetration.

EN 374-4:2013 is a European standard for gloves that protect against microorganisms. It sets rules for how the gloves should protect against microorganisms and how to test if they meet the standards. Gloves that pass the tests can have a label that says they meet the standard. The test results can be pass or fail for each test that checks the gloves resistance to microorganisms.

EN 374-1:1996 is a European standard that specifies the performance requirements and test methods for chemical protective gloves. It defines the minimum requirements for gloves to protect against chemicals and microorganisms. The standard includes test methods for permeation resistance, degradation, and penetration. Possible test results include pass/fail for each requirement.

EN 374-1:1995 is a standard that specifies the performance requirements and test methods for chemical protective gloves. It defines the minimum requirements for gloves to protect against chemicals and microorganisms. The standard includes test methods for permeation resistance, degradation, and penetration. Possible test results include pass/fail for each requirement.

EN 374-1:2004 is a European standard that defines the performance requirements and test methods for chemical protective gloves. It specifies the minimum requirements for gloves that protect against chemicals and microorganisms. The standard includes tests for permeation resistance, degradation, and penetration. Possible test results include pass/fail for each requirement.

EN 374-1:2005 is a European standard that specifies the performance requirements and test methods for chemical protective gloves. It defines the minimum requirements for gloves that protect against chemicals and microorganisms. The standard includes tests for permeation resistance, degradation, and penetration. Possible test results include pass/fail for each requirement.

EN 374-1:1994 is a European standard for the performance of chemical protective gloves. It includes requirements for things like penetration, permeation, and degradation resistance, as well as testing methods to ensure that the gloves meet those requirements. Possible test results would include things like the amount of chemical resistance of the gloves, and the amount of time the gloves can be worn before needing to be replaced.

EN 374-1:2003 is a European standard that specifies the performance requirements and test methods for chemical protective gloves. It defines the minimum requirements for gloves to protect against chemicals and microorganisms. The standard includes test methods for permeation resistance, degradation, and penetration. Possible test results include pass/fail for each requirement.

EN ISO 374-1:2016 is a standard that defines the performance requirements for gloves that protect against chemicals and microorganisms. The standard specifies the design, materials, and testing requirements for gloves to protect against chemicals and microorganisms. Possible test results include measurements of the gloves' permeation resistance, degradation, and penetration. It also includes the safety and functionality requirements for gloves.

EN ISO 374-1:2016/A1:2018 is a standard that sets the rules for gloves that protect against dangerous chemicals and microorganisms. It says how gloves should be made, what materials should be used, and how they should be tested. Possible test results include how well the gloves keep out chemicals, how long they last and how well they protect the hands. This amendment updates the original standard with new requirements.

CE Marking is a label that shows a product meets certain safety and environmental standards set by the European Union. To get the CE Marking, a company must test and certify their product meets these standards. CE Marking is required for many products sold in the EU, including electronics, machinery, toys and medical devices. It helps ensure that products are safe for consumers and the environment, and allows for easy trade within the EU.

Food safe refers to the safety of food products that are used or consumed by people. In Europe, food safety is regulated by the European Union (EU) and the European Food Safety Authority (EFSA). These organizations set standards and requirements for food products to ensure they are safe to eat. To be considered "food safe" in Europe, a product must meet these standards and be free of harmful substances. This includes being free of harmful bacteria, pesticides, and other contaminants. Food products that do not meet these standards cannot be sold or used in the EU.

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.

PPE stands for "personal protective equipment." PPE Category 3 refers to equipment that is complex and provide the highest level of protection such as powered respirators, SCBA, and full body suits. In Europe, PPE Category 3 must meet certain safety standards set by the European Union, which means that it must be designed and manufactured to protect the user without causing harm. Companies that make or sell PPE must prove that it meets these standards. They also must have a quality management system in place, have to be audited regularly by a notified body and have to have a technical documentation.

BODY PRODUCTS RELAX Pharma und Kosmetik GmbH is a renowned name in the healthcare and cosmetics industry. For years, they have been a trusted supplier of high-quality gloves, including nitrile and vinyl gloves, catering to a wide range of professional sectors. Their commitment to quality and safety has positioned them as a market leader in the provision of essential protective wear. With a rich history and a reputation for excellence, they continue to serve their European audience with unwavering dedication. BODY PRODUCTS RELAX Pharma und Kosmetik GmbH stands as a testament to the power of reliability and industry expertise.

Gloves are a type of clothing worn on the hands. Leather. Gloves are used in many jobs. They are used in the medical field, in the food industry, in the automotive industry, and in many other industries.

Shipping supplies are the materials that are used to ship goods. They are typically made of cardboard, plastic or sustainable materials. Shipping supplies are used by companies that ship products.

Safety equipment is any device or object that is used to protect a person from injury or death. These equipment are typically made of rubber, plastic, or metal. Jobs that use safety equipment include construction workers, firefighters, police officers, and many others.

Clothing is a covering for the body and are typically made of fabric. They are used in the medical field, in the food industry, in the automotive industry, and in many other industries.

Food and utensils are the things you use to eat and drink. They are typically made of metal, glass, plastic, or wood. Food and utensils are used in the preparation and serving of food.

Cleaning and hygiene supplies are products used to clean and maintain hygiene. Cleaning and hygiene supplies are typically made of plastic, metal, or paper. Cleaning and hygiene supplies are used by janitors, maids, and other people who work in the cleaning industry.

Tools, Tapes & Bolts are the items that are used to assemble the parts of a product and are typically made of metal or plastic. Jobs that use these parts are those that require the use of hand tools to complete the job.

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