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.

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 455-1:2020+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 455-1:2020+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 455-1:2000 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 455-1:1993/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 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 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 420:2003 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 420:1994 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 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 374-1:2004 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 374-1:1996 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 374-1:2005 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 374-1:1995 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 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.

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 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.

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.

Headquartered in Plovdiv, Bulgaria, Aldena is a recognized leader in high-quality disposable latex, vinyl and nitrile gloves. Aldena has met the needs of thousands of professionals for over ten years in the medical, dental, healthcare, laboratory, to name a few. Over the years, Aldena has carved out a significant niche for itself and is now recognised as a market leader. Trust and customer satisfaction remain at the core of Aldena's operations, fostering an environment of continued growth and innovation.

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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