WeeSafe Weepro Labo Integral Coverall Type 5/6, White

Standards and labels

• EN ISO 13982-1:2004

  Chemical protective clothing, like coveralls and suits, with the EN ISO 13982-1:2004 rating are tested for resistance against penetration by airborne solid particles and for robust seam integrity. This ensures the clothing provides reliable full-body protection from hazardous dusts and fine dry chemicals.

  Test results

  Airborne Solid Particle Protection Type 5

  This full-body suit protects you from hazardous airborne solid particles like dust and fibres. It's ideal for tasks such as asbestos removal, pharmaceutical work, or any job where you are exposed to harmful dry particulates.

• EN 13034:2005

  Protective clothing, such as coveralls and aprons, with the EN 13034:2005 rating are tested for limited protection against light spray, liquid aerosols, or low-volume splashes of liquid chemicals. This means the clothing provides a barrier against minor chemical exposure, allowing you time to safely remove it before chemicals penetrate.

  Test results

  Liquid Chemical Protection Type 6

  Provides protection against light sprays, liquid aerosols, and low-pressure, low-volume splashes of liquid chemicals. It is intended for use in low-risk situations where a full chemical barrier is not required, such as industrial cleaning or maintenance.

• EN 13688:2013/A1:2021

  Protective clothing with the EN 13688:2013/A1:2021 rating are tested for general requirements including comfort, harmlessness of materials, proper sizing, and durability. This ensures the garment is safe, fits well, won't cause irritation, and maintains its quality over time for your protection.

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• EN 13274-4:2001

  Respiratory protective devices with the EN 13274-4:2001 rating are tested for resistance to flame and flammability. This means the device has been evaluated to help ensure its safety when exposed to fire.

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• EN 863:1995

  Protective clothing and materials with the EN 863:1995 rating are tested for puncture resistance. This measures the maximum force needed to push a sharp spike through the material, helping you choose clothing that protects against penetration by sharp objects.

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• EN ISO 12947-2:1998

  Textile fabrics, such as those used in upholstery and clothing, with the EN ISO 12947-2:1998 rating are tested for their abrasion resistance using the Martindale method, measuring how many rubs they endure before showing signs of breakdown. This indicates the fabric's durability, helping you choose products that will withstand wear and tear and maintain their appearance longer.

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• EN ISO 13934-1:1999

  Textile fabrics with the EN ISO 13934-1:1999 rating are tested for their tensile strength and how much they stretch before breaking. This ensures the fabric's durability and resistance to tearing, leading to longer-lasting products.

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• EN ISO 13935-2:1999

  Textile products and clothing with the EN ISO 13935-2:1999 rating are tested for the maximum force their sewn seams can withstand before breaking. This ensures the seams are strong and durable, giving you more reliable and longer-lasting items.

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• EN ISO 7854:1997

  Rubber- or plastics-coated fabric products with the EN ISO 7854:1997 rating are tested for their resistance to damage from repeated flexing. This means the material has been assessed for how well it withstands bending and crumpling over time, indicating its durability and ability to maintain its integrity with use.

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• EN ISO 9073-4:1997

  Nonwoven products with the EN ISO 9073-4:1997 rating are tested for their resistance to tearing using a standard method. This ensures the material is durable, providing better reliability and a longer lifespan for the product during everyday use.

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• 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.

• 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.