The European Regulation (EU) 2016/425 defines the fundamental requirements for PPE (Personal Protective Equipment) to ensure maximum safety for those who use them. The objective of this regulation is to guarantee a safe working environment for PPE users and public health.
European Regulation (EU) 2016/425 (which repealed and replaced the previous EEC Directive 89/686/ EEC on Personal Protective Equipment) requires that all PPE be marked according to its relevant category. The marking may appear directly on the PPE or, if this is not feasible, on the packaging, using symbols and information regarding the PPE’s performance levels and characteristics.
CATEGORY I – Minimal risks
Requirements for the manufacturer
Self-certification
CATEGORY II – Intermediate level risks
Certification by accredited certified body
CATEGORY III – Irreversible or life-threatening risks
Certification by an accredited certification body; third-party verification of the manufacturing process and the suitability of PPE.
The number of the accredited certification body must be indicated next to the CE mark (e.g., 0123)
