Personal Protective Equipment
Products in this section have been carefully selected to offer a good range that complies with Directives 89/686/EEC1 - PPE (Personal Protective Equipment) and Regulation (EU) 2016/425 on Personal Protective Equipment (PPE). Under these directives the basic health and safety requirements are adhered to by working to the European standards, which set the highest possible requirements and do not allow for additional national provisions within that standard, thereby setting minimum European standards.
On the 21st April 2018, Regulation (EU) 2016/425 on Personal Protective Equipment (PPE) came into force and replaced the old PPE Directive 89/686/EEC.
PPE is defined as products that the user can wear or hold, in order to be protected against hazards either at home, at work or whilst engaging in leisure activities.
Main Changes in Regulation (EU) 2016/425
The new Regulation now applies to the whole supply chain rather than just manufacturers. Everyone involved in the manufacture, supply and distribution of PPE must ensure their PPE meets with the standard requirements.
Some of the standard requirements are outlined below:
In certain cases, the manufacturer’s obligations can now apply to importers and distributors. An importer or distributor who markets a product in Europe under their own name, brand or trademark becomes liable for the full manufacturer’s obligations.
Regulation (EU) 2016/425 slightly modifies the risk categorisation of products. Life Jackets and hearing protection are moved from Category II (Intermediate PPE) to Category III (Complex PPE). This means that they are now subject to stricter conformity assessment procedures and ongoing surveillance.
There was a transition period of 1 year (21st April 2018 to 20th April 2019) where both the old Directive and the new Regulation are applicable. Therefore PPE designed and manufactured in accordance with Directive 89/686/EEC could still be placed on the market until 21st April 2019.
EC type-examination certificates and approval decisions issued under the old Directive shall remain valid until 21st April 2023 unless they expire before that date.
Regulation (EU) 2016/425 does not apply any duties directly to end users of PPE. Employers who are selecting and using PPE within their own organisation are covered by the Personal Protective Equipment at Work Regulations 1992 which are unaltered by this Regulation. Those involved in specifying, sourcing or purchasing PPE for use within their own organisation should continue to select appropriate PPE which has been CE marked.
In the UK The Personal Protective Equipment (Enforcement) Regulations 2018 (SI 2018/390) provide an enforcement and penalty regime for Regulation (EU) 2016/425.
CE implies that the PPE complies with the basic requirements laid down by the EEC directive: Personal Protective Equipment
SIMPLE DESIGN (CATEGORY 1)
Simple Design - for minimal risks only. Suitable only for low risk applications where hazards can be identified by the wearer in time to deal with them.
INTERMEDIATE DESIGN (CATEGORY 2)
Intermediate Design - reversible risks. Products are type examined by an approved body where they examine the manufacturers’ technical specifications and conduct tests for the relevant standards to ascertain their conformity and/or performance.
COMPLEX DESIGN (CATEGORY 3)
Potentially fatal risks, for example in activities where toxic or highly corrosive chemicals are handled. The Personal Protective Equipment must meet the standards set out for this category. Its compliance is not only certified but also checked by a notified body, the reference number of which is located below the CE logo.