BS EN 13200-3:2018 - Spectator facilities. Separating elements. Requirements

BS EN 13200-3:2018

Spectator facilities. Separating elements. Requirements

Status : Current   Published : September 2018



This document specifies design requirements for layout and product characteristics for separating elements within spectator accommodation at permanent or temporary entertainment venues including sport stadia, sport halls, indoor and outdoor facilities for the purpose of enabling their functionality. Other permanent venues such as theatres, cinemas, opera houses, lecture halls and similar are excluded from this document. Elements and barriers included in this document are: - barrier front of a row of fixed seats; - barrier adjacent to end row of seats; - barrier behind a rear row of seats; - barrier at the foot of a gangway or on stairway, aligned at right angles to the direction of movement; - side or lateral barrier, aligned parallel to the direction of spectator movement; - gangway barriers; - gangway barriers in standing areas, aligned at right angles to the direction of spectator movement; - crush barriers; - barriers for spectator galleries; - external perimeter barriers and barriers between sectors.

Standard NumberBS EN 13200-3:2018
TitleSpectator facilities. Separating elements. Requirements
Publication Date19 September 2018
Normative References(Required to achieve compliance to this standard)EN 13200-1:2012, EN 1991-1-1, EN 13200-7
Informative References(Provided for Information)No other standards are informatively referenced
ReplacesBS EN 13200-3:2005
International RelationshipsEN 13200-3:2018
Draft Superseded By16/30341237 DC
DescriptorsCrush barriers, Spectator facilities, Construction works, Buildings open to the public, Sports facilities, Safety devices, Protective barriers, Layout, Stadia, Assembly facilities, Crowd safety, Entertainment facilities
Title in FrenchInstallations pour spectateurs Éléments de séparation. Exigences
Title in GermanZuschaueranlagen Abschrankungen. Anforderungen
ISBN978 0 580 94200 6
File Size973 KB

 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents

Tracked Changes

Understand the changes made to a standard with our new Tracked Changes version

Develop a PAS

Develop a fast-track standardization document in 9-12 months

Worldwide Standards
We can source any standard from anywhere in the world