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This document applies to Recirculatory Filtration Fume Cupboards (RFFC). Recirculation Filtration Fume Cupboards are devices intended to protect their users by means of: - the ability to contain potentially hazardous materials; - the ability to remove potentially hazardous materials from air exhausted from within the fume cupboard by means of filtration before the air is recirculated (to the room in which the fume cupboard is located). This document includes design and manufacturing requirements together with type testing procedures.

This document applies to workbenches, movable science tables and workbench shelves designed for use in educational institutions and similar laboratories. This European Standard specifies safety and durability requirements and test methods and gives dimensions. Requirements and test methods related to the fire safety or workbenches and to the resistance of the work surface are not included in this European Standard. Requirements concerning electrical safety are not included. Annex A (normative) Durability tests.

This document specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant products intended to be used for treatment in aqueous systems against Legionella pneumophila that form a homogeneous, physically stable preparation when diluted with buffered ferrous hard water or hard water. Whenever Legionella pneumophila poses a risk to human health, this method is suitable for water used in cooling towers and water for general purposes, like spas, pools, showers and other uses. The method is not suitable for electro-chemical disinfection. The European Standard applies to products used as a single application shock treatment in order to kill Legionella pneumophila. It is not suitable for the evaluation of those products that are dosed continuously in to water systems to control the growth of Legionella pneumophila. NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 This method corresponds to a phase 2 step 1 test. NOTE 3 This method does not take into account the fact that Legionella pneumophila is often found in cells of amoebae and/or biofilms and that thereby a product’s activity against the bacteria may be reduced. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendation".

This document is a product specification, giving performance requirements for water overhead emergency safety body showers installed on industrial and logistic sites, (in combination with safety eyewashes and hand-held showers as well), a) which are permanently connected to a water supply or b) which are equipped with a store tank and optionally connected to an uninterrupted or a temporary water supply. Emergency safety body showers using fluid other than water are not considered in this standard. This standard also specifies requirements in respect of installation, adjustment and marking of the showers as well as operation and maintenance instructions to be given by the manufacturer. NOTE 1 Plumbed-in body showers designed for laboratory facilities are dealt with in EN 15154-1. NOTE 2 Water multiple nozzle body showers for sites other than laboratories are dealt with in prEN 15154-6. NOTE 3 Attention is drawn to national regulations which may apply in respect of the installation and use of emergency safety showers

This document is a product specification, giving performance requirements for plumbed-in multiple nozzle emergency safety body showers which are permanently connected to a water supply and installed on industrial and logistic sites. Emergency safety body showers using fluid other than water are not considered in this standard. This standard also specifies requirements in respect of installation, adjustment and marking of the showers as well as operation and maintenance instructions to be given by the manufacturer. NOTE 1 Plumbed-in emergency safety body showers designed for laboratory facilities are dealt with in EN 15154-1. NOTE 2 Water overhead body showers for sites other than laboratories are dealt with in prEN 15154-5. NOTE 3 Attention is drawn to national regulations which may apply in respect of the installation and use of emergency safety showers.

This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water or - in the case of ready-to-use products - with water. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance. This document applies to products that are used in food, industrial, domestic and institutional areas excluding areas and situations where disinfection is medically indicated and excluding products used on living tissues except those for hand hygiene in the above considered areas. The following areas are at least included: a) processing, distribution and retailing of: 1) food of animal origin:  milk and milk products;  meat and meat products;  fish, seafood, and related products;  eggs and egg products;  animal feeds;  etc. 2) food of vegetable origin:  beverages;  fruits, vegetables and derivatives (including sugar, distillery, etc.);  flour, milling and baking;  animal feeds;  etc. b) institutional and domestic areas:  catering establishments;  public areas;  public transports;  schools;  nurseries;  shops;  sports rooms;  waste containers (bins, etc.);  hotels;  dwellings;  clinically non sensitive areas of hospitals;  offices;  etc. c) other industrial areas:  packaging material;  biotechnology (yeast, proteins, enzymes, etc.);  pharmaceutical;  cosmetics and toiletries;  textiles;  space industry, computer industry;  etc. EN 14885 specifies in detail the relationship of the various tests to one another and to “use recommendations”. NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 This method corresponds to a phase 2 step 1 test.