Hygostar Chemical Star Protection Kit

Standards and labels

• EN 455-2:1995

  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.

  Test results

  Physical Properties Tested

  The European standard EN 455-2:1995 deals with the requirements and testing for physical properties of medical gloves. This test evaluates the physical strength and durability of gloves to ensure they are safe for use in medical settings. The specified test result from EN 455-2:1995, such as tensile strength and elongation, indicates how much force a glove can withstand before breaking and how much it can stretch, respectively. The test methods typically involve applying a force to a glove material to measure its tensile strength and elongation. These measured properties help classify gloves' suitability for various medical tasks, providing critical information for users regarding the gloves' resilience and flexibility. Thus, manufacturers and procurement professionals can use this metric to assess the quality and appropriateness of medical gloves for specific applications, ensuring safety and compliance with EU regulations in medical environments.

• EN 420:2003+A1:2009

  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.

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• EN 14605:2005

  EN 14605:2005 is a European standard that sets rules for how certain types of protective clothing should be tested and what requirements they must meet in order to be considered safe and effective against chemical hazards. The standard covers the test methods and performance requirements for chemical protective clothing such as coveralls, gloves, boots and overalls. The standard also sets requirement for labeling, packaging and storage of these clothing. Tests must be done to make sure the protective clothing meets the standard. If the protective clothing pass the tests, they are considered good to use.

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• EN 13034:2005

  EN 13034:2005 is a European standard that specifies the requirements and test methods for Type 6 protective clothing designed to provide protection against liquid chemicals. This standard sets criteria for the fabric's resistance to penetration by liquid chemicals and establishes guidelines for the overall design and construction of the clothing. It ensures that Type 6 protective clothing offers reliable protection for workers in industries where they may be exposed to liquid chemical hazards, but it may not be suitable for protection against airborne particles.

  Test results

  Liquid Chemical Protection Type 6 PB

  EN 13034:2005 specifies the performance requirements for protective clothing that offers limited protection against liquid chemicals, identified specifically as Type 6 PB (partial body protection). The 'Type 6 PB' designation implies that the protective garment has been tested and confirmed to provide effective defense against light spray and minor splashes of liquid chemicals, but only for parts of the body such as aprons, sleeves, or boots rather than full body suits. This standard tests the fabric's barrier effectiveness by applying a defined volume of liquid to the garment and assessing any penetration or repellence under controlled laboratory conditions. Garments achieving Type 6 PB classification are crucial for tasks in industries like chemical processing or handling where full body coverage is unnecessary, thereby offering flexibility and targeted protection, reducing the risk of chemical exposure to critical areas of the body.

• EN 374-5:2016

  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.

  Test results

  Micro-organisms Virus

  EN 374-5:2016 is a standard that outlines the requirements and testing methods for protective gloves designed to protect against viruses. The designation 'Virus' indicates that the gloves have passed specific tests confirming their barrier effectiveness against viruses. These tests involve assessing the glove material's resistance to penetration by blood-borne pathogens and other virus-containing fluids, using a bacteriophage as a surrogate virus due to its small size and resistance. Gloves that meet this standard are vital in healthcare settings, laboratories, and any environment where there is a risk of exposure to viral infections. They are crucial for preventing the transmission of diseases, ensuring that workers are protected when handling potentially infectious materials, thus enhancing safety and health protocols in workplaces with biological hazards.

• EN 455-4:2009

  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.

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• EN 455-1:1993

  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.

  Test results

  Tightness AQL #,##

  EN 455-1:1993 sets the standards for medical gloves for single use, focusing on freedom from holes and ensuring glove integrity. The 'Tightness' test result, indicated by an Acceptable Quality Level (AQL) value, measures the quality level acceptable for the pinhole rate in glove batches. A lower AQL value, such as 1.5, typically used in medical settings, signifies a higher level of quality control where fewer gloves with defects are allowed. The testing for this standard involves randomly selecting gloves from a batch and filling them with water to check for leaks. Gloves that pass this test at a certain AQL value are deemed safe for use in medical and surgical procedures, where maintaining a sterile environment is crucial to prevent contamination and infection. This certification ensures that users can rely on the protective barrier of the gloves against pathogens and other contaminants.

• EN 1149-5:2008

  EN 1149-5:2008 is a European standard that specifies the requirements for electrostatic dissipative (ESD) gloves. The standard defines performance requirements for material, design, and testing of ESD gloves. The gloves must be able to effectively discharge static electricity and protect the wearer from ESD. Testing includes measuring the surface resistance of the glove material. Pass/fail results are based on the gloves meeting or not meeting the specified requirements.

  Test results

  Material Performance Tested

  The EN 1149-5:2008 standard specifies the performance requirements for material used in protective clothing designed to avoid incendiary discharges. The test result Tested means that the material has undergone relevant evaluation procedures to confirm its static dissipative properties. These tests generally involve measuring the electrical resistance of the material in ohms (Ω) to determine its capability to dissipate electrostatic charges and prevent sparking that could ignite flammable substances. The practical implications of this result for the respective product category (like protective workwear for use in explosive atmospheres) are significant, as it ensures that the clothing provides a level of protection against electrostatic discharges, potentially reducing the risk of fire or explosion in environments with flammable gases, vapors, or dusts.

• EN 149:2001/AC:2002

  EN 149:2001/AC:2002 is a European standard for filtering half masks for protecting against particles and it is an amendment of EN 149:2001. It outlines additional requirements for mask design and performance testing. The mask must be able to filter a certain percentage of particles and have good breathability. The test results shows how well the mask filters and how easy it is to breathe through. It also specifies the mask's ability to filter out specific airborne particles like dust, mist, and fumes. It includes additional requirements for the performance of the mask, such as the ability to seal against the face and the mask's durability.

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• EN 455-3:1999

  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.

  Test results

  Biological Evaluation Tested

  The EN 455-3:1999 standard evaluates the biological safety of medical gloves for single use. It focuses on tests that determine acceptable levels of endotoxins, protein content to minimize allergic reactions, and leachable substances which could have harmful effects. Essentially, the test results from EN 455-3:1999 determine if the tested gloves release any potential allergens or toxic chemicals that could harm users, ensuring product safety in regards to biological factors.

• EN 1073-2:2002

  EN 1073-2:2002 is a European standard that defines the requirements for measuring and evaluating the resistance of textiles to penetration of airborne radioactive particles. The standard includes procedures for measuring the ability of textile materials to prevent the penetration of radioactive particles through the fabric. The performance requirements specify the conditions for testing, as well as the evaluation criteria for determining resistance. Possible test results include a rating on a scale of 1-5, with 5 indicating the highest level of resistance to particle penetration.

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• EN ISO 13982-1:2004

  EN ISO 13982-1:2004 is a European standard that specifies the requirements and test methods for Type 5 protective clothing designed to protect against airborne solid particles. It sets criteria for material resistance and construction to prevent penetration of hazardous particles such as dust, fibers, and powders. The standard ensures that the garments provide effective protection in industries where workers may be exposed to such particles, but it should not be relied upon for protection against liquid chemicals or vapors.

  Test results

  Airborne Solid Particle Protection Type 5

• EN ISO 374-1:2016

  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.

  Test results

  Specified Requirements Type A

• EN 14126:2003/AC:2004

  EN 14126:2003, along with the amendment AC:2004, is a European standard that specifically addresses protective clothing designed to provide protection against infectious agents, including viruses and bacteria. The standard outlines the requirements and test methods for evaluating the material's resistance to penetration by microorganisms. The amendment AC:2004 introduces updates and refinements to enhance the performance and reliability of the protective clothing, ensuring improved protection for individuals exposed to biological hazards. Compliance with EN 14126:2003 and its amendment ensures that the protective clothing meets the necessary standards for barrier protection against infectious agents.

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• 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.

• Food Safe

  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 Label

  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 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.