SIST EN 60601-2-29:2009/A11:2012
(Amendment)Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators
Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of RADIOTHERAPY SIMULATORS, hereafter referred to as ME EQUIPMENT. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.
Medizinische elektrische Geräte - Teil 2-29: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Strahlentherapiesimulatoren
Appareils électromédicaux - Partie 2-29: Exigences particulières pour la sécurité de base et les performances essentielles des simulateurs de radiothérapie
Medicinska električna oprema - 2-29. del: Posebne zahteve za osnovno varnost in bistvene lastnosti radioterapevtskih simulatorjev
Ta mednarodni standard velja za OSNOVNO VARNOST in BISTVENE LASTNOSTI RADIOTERAPEVTSKIH SIMULATORJEV, v nadaljevanju ME OPREMA. Če bo točka ali podtočka izrecno namenjena samo uporabi za ME OPREMO ali samo za ME SISTEME, bosta naslov in vsebina te točke ali podtočke to tudi navedla. Sicer točka in podtočka veljata za ustrezno ME OPREMO in ME SISTEME. NEVARNOSTI, ki so del fiziološkega delovanja ME OPREME ali ME SISTEMOV v okviru uporabe tega standarda, niso zajete s posebnimi zahtevami tega standarda, razen v točkah 7.2.13 in 8.4.1 splošnega standarda.
General Information
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Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN 60601-2-29:2009/A11:2012
01-januar-2012
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQH]DKWHYH]DRVQRYQRYDUQRVWLQ
ELVWYHQHODVWQRVWLUDGLRWHUDSHYWVNLKVLPXODWRUMHY
Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and
essential performance of radiotherapy simulators
Medizinische elektrische Geräte - Teil 2-29: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Strahlentherapiesimulatoren
Appareils électromédicaux - Partie 2-29: Exigences particulières pour la sécurité de base
et les performances essentielles des simulateurs de radiothérapie
Ta slovenski standard je istoveten z: EN 60601-2-29:2008/A11:2011
ICS:
11.040.60 Terapevtska oprema Therapy equipment
SIST EN 60601-2-29:2009/A11:2012 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN 60601-2-29:2009/A11:2012
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SIST EN 60601-2-29:2009/A11:2012
EUROPEAN STANDARD
EN 60601-2-29/A11
NORME EUROPÉENNE
October 2011
EUROPÄISCHE NORM
ICS 11.040.60
English version
Medical electrical equipment -
Part 2-29: Particular requirements for the basic safety and essential
performance of radiotherapy simulators
Appareils électromédicaux - Medizinische elektrische Geräte -
Partie 2-29: Exigences particulières pour Teil 2-29: Besondere Festlegungen für die
la sécurité de base et les performances Sicherheit einschließlich der wesentlichen
essentielles des simulateurs de Leistungsmerkmale von
radiothérapie Strahlentherapiesimulatoren
This amendment A11 modifies the European Standard EN 60601-2-29:2008; it was approved by CENELEC on
2011-10-01. CENELEC members are bound to comply with the CEN/CENELEC Internal Regulations which
stipulate the conditions for giving this amendment 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 CENELEC member.
This amendment exists in three official versions (English, French, German). A version in any other language
made by translation under the responsibility of a CENELEC member into its own language and notified to the
CEN-CENELEC Management Centre has the same status as the official versions.
CENELEC members a
...
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