EN 1865-2:2010+A1:2015

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Oprema za ravnanje s pacienti v reševalnih vozilih - 2. del: Nosila s pomožnim pogonomKrankentransportmittel im Krankenkraftwagen - Teil 2: Kraftunterstützte KrankentrageSpécifications d'équipements pour le transport de patient dans les ambulances routières - Partie 2: Brancard motoriséPatient handling equipment used in road ambulances - Part 2: Power assisted stretcher43.160Vozila za posebne nameneSpecial purpose vehicles11.160First aidICS:Ta slovenski standard je istoveten z:EN 1865-2:2010+A1:2015SIST EN 1865-2:2010+A1:2015en,de01-maj-2015SIST EN 1865-2:2010+A1:2015SLOVENSKI
STANDARDSIST EN 1865-2:20101DGRPHãþD

EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM
EN 1865-2:2010+A1
March 2015 ICS 11.160 Supersedes EN 1865-2:2010English Version
Patient handling equipment used in road ambulances - Part 2: Power assisted stretcher
Spécifications d'équipements pour le transport de patient dans les ambulances routières - Partie 2: Brancard motorisé
Krankentransportmittel im Krankenkraftwagen - Teil 2: Kraftunterstützte Krankentrage This European Standard was approved by CEN on 2 July 2010 and includes Amendment 1 approved by CEN on 20 December 2014.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom.
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Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC on Medical Devices and of EU Directive 2006/42/EC on Essential Health and Safety Requirements" . 10 Bibliography . 12
width: !(550 ± 6020+−) mm" ;
height: maximum 300 mm from loading holding assembly to unloaded lying part. This height dimension does not apply to stretchers with monoblock undercarriages. If a monoblock is not available, the stretcher shall be constructed such that it is detachable from the undercarriage. Where a stretcher support is used the measurement shall be taken from the top surface of the stretcher support to the lying part of the stretcher. — Undercarriage: length and width of the frame of the undercarriage when located in the ambulance shall not exceed length and width of the stretcher. 4.2.3 Mass The total mass excluding mattress and patient restraints shall be not more than !75 kg". NOTE In all cases the mass should be as low as possible. SIST EN 1865-2:2010+A1:2015

150 mm and 200 mm measured from the top of the stretcher frame to the top of the side rail. b) If longitudinal handles are incorporated they shall be fitted to the ends of the longitudinal frame such that they lock and do not twist when they are stowed or in use. They shall be designed to minimize the risk of injuries to the hands and wrists when being operated or the stretcher is carried at angles. It shall allow the fixation and use of a carrying harness. c) The stretcher shall have a water and scratch resistant paint finish or be manufactured of corrosion resistant material. Both shall be unaffected by disinfectants. d) If intended to be used without un
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