Protective clothing with the EN 14325:2004 rating are tested for the physical performance of their materials, seams, and joins, including resistance to abrasion, tearing, and chemical penetration. This ensures you can compare and choose garments that provide the appropriate level of protection against various chemical hazards.

Protective clothing with the EN 13688:2013 rating are tested for general requirements like ergonomics, harmlessness, accurate sizing, durability after cleaning, and clear labeling. This ensures the clothing is safe, comfortable, fits well, and provides reliable, long-lasting protection with clear user instructions.

Protective clothing with the EN 14126:2003/AC:2004 rating is tested for resistance against penetration by contaminated liquids, aerosols, and solid particles containing infective agents. This ensures the material provides a barrier against biological hazards, offering you trusted protection in risky environments.

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.