About Optifora

What are the PPE declaration of conformity and marking for?

The marking is the manufacturer's declaration that the product was placed on the market in accordance with the legislation; it is not a grade of quality. The real information is in the declaration of conformity: the product's category, the standards it was assessed against, and — for categories II and III — the notified body that carried out type examination. Where the purchase record is not kept with that document, what risk the item was bought for cannot be shown later.

What the marking says, and what it does not

The conformity marking on a product is the manufacturer's declaration that “this product meets the requirements of the relevant legislation”. It is not a quality star, a performance grade or a recommendation. Nor does it say which risk the product protects against, or how much: that is what the standard number and the performance class say.

The real document: the declaration of conformity

It comes with the product and contains:

  • the manufacturer and product identity,
  • the product's category,
  • the harmonised standards applied,
  • for categories II and III, the notified body that carried out type examination,
  • for category III, the body carrying out production surveillance.

In an inspection, and after an accident, this document is the only written answer to “which risk was this equipment chosen for”.

Instructions are mandatory too

The product must be accompanied by information on use, storage, cleaning, maintenance and service life, in a language the user understands. Equipment delivered without instructions is delivered incomplete.

What purchasing should do

The declaration and the instructions must be attached to the product record at the moment of purchase. Asking the supplier afterwards usually fails: the model changes, the supplier changes, the version of the document changes. Where the inventory holds the standard, the category and the document beside the product, a withdrawal or a finding can be traced to every affected item with a single query.

Manage this in Optifora

Optifora is not a single program but a compliance platform assembled from modules. The catalogue states which module is ready today and which is on the roadmap.

See what Optifora is