Standards and labels

• EN 556-1:2001

  EN 556-1:2001 is a standard that explains how to sterilize medical equipment using steam. It tells you what temperature and pressure should be used during the sterilization process. The test results will show if the equipment is completely clean and free of germs, and if the sterilization process was done correctly.

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• EN ISO 374-1:2016

  Test results

  Specified Requirements Type B

  The EN ISO 374-1:2016 standard specifies requirements for gloves intended to protect against chemicals and micro-organisms. A glove that achieves a Type B test result in this standard offers resistance to at least three chemicals, with a breakthrough time of at least 30 minutes for each chemical tested. This test involves subjecting the gloves to chemicals and measuring the time it takes for the chemicals to penetrate through the material. Practical implications for this test result entail selecting gloves categorized under Type B for environments where exposure to specific hazardous chemicals for durations not exceeding 30 minutes is anticipated. This makes the gloves suitable for certain chemical handling tasks within specified limits, assuring a protective barrier during the exposure period.

• EN ISO 374-5:2016

  Test results

  Micro-organisms Bacteria & Fungi

  EN ISO 374-5:2016 is a standard that defines the requirements for gloves to protect against dangerous chemicals and micro-organisms, including bacteria and fungi. The test results indicating protection against Bacteria & Fungi confirm that the gloves have effectively passed the necessary evaluations to guard against these types of micro-organisms. The test method used assesses the glove's resistance to penetration and permeation by micro-organisms. The glove material undergoes specific challenges designed to ensure that pathogens such as bacteria and fungi cannot penetrate or permeate through the material under standard testing conditions. Practical implications of these results include assurance that gloves certified under this standard provide health professionals and others exposed to biohazards with a reliable barrier against potential infections caused by bacteria and fungi, which is crucial for both healthcare settings and lab environments.

• EN ISO 21420:2020

  Test results

  General Requirements Guide

  EN ISO 21420:2020 is a standard that outlines general requirements and guidelines for protective gloves, aiming to ensure their quality, performance, and suitability for various applications. When a product meets the requirements outlined in the General Requirements section of EN ISO 21420:2020, it signifies that the gloves comply with fundamental quality and performance criteria, including factors such as size, fit, ergonomics, and dexterity. The practical implications of this compliance are significant, as it assures users of the gloves' basic functionality and suitability for general hand protection purposes across a range of industries and applications. The test method involves evaluating various aspects of the gloves, including dimensions, construction, materials, and labeling, to ensure conformity with the specified requirements. Compliance with these general requirements enhances user confidence in the protective gloves' reliability and effectiveness, promoting workplace safety and facilitating compliance with regulatory standards.

• EN 421:2010

  EN 421:2010 is a European standard that specifies requirements and test methods for gloves to protect against ionizing radiation and radioactive contamination. The standard is applicable to gloves offering protection to the hand and various parts of the arm and shoulder. It applies also to gloves to be mounted in permanent containment enclosures.

  Test results

  Radiation & Contamination Tested

  EN 421:2010 is a European standard designed to address radiation protection for protective clothing. Its purpose is to ensure that protective clothing worn in environments where there is a risk of radiation exposure provides adequate protection to the wearer. One of the critical aspects tested under this standard is the resistance of the protective clothing to penetration by radioactive contamination. This test result signifies the ability of the clothing to prevent radioactive particles from reaching the wearer's skin, thereby minimizing the risk of contamination and radiation exposure. The test method involves exposing the protective clothing to a specific level of radioactive contamination and then assessing whether any penetration occurs. Practical implications of this result for the product category include ensuring that protective clothing meets stringent safety standards, thereby safeguarding the health and well-being of individuals working in radiation-prone environments such as nuclear facilities or medical facilities handling radioactive materials.

• CE Marking

  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.

• PPE Category 3

  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.