EN 60601-2-49:2001
(Main)Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment
Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment
Specifies requirements for the safety of multifunction patient monitoring equipment. Multifunction patient monitoring equipment is defined as a modular or pre-configured device including more than one physiological monitoring unit designed to collect information from a single patient and process it for monitoring purposes and to generate alarms.
Medizinische elektrische Geräte - Teil 2-49: Besondere Festlegungen für die Sicherheit von multifunktionalen Patientenüberwachungsgeräten
Appareils électromédicaux - Partie 2-49: Règles particulières de sécurité des appareils de surveillance multifonction des patients
Spécifie des exigences de sécurité pour les appareils de surveillance multifonction des patients. Le domaine d'application de la présente norme est restreint aux appareils qui comportent soit plusieurs parties appliquées, soit plusieurs fonctions uniques, destinés à la connexion à un patient unique. C'est la version bilingue de la version anglaise publiée en Juillet 2001.
Medicinska električna oprema - 2-49. del: Posebne varnostne zahteve za pacientovo večfunkcijsko nadzorovalno opremo (IEC 60601-2-49:2001)
General Information
- Status
- Withdrawn
- Publication Date
- 25-Oct-2001
- Withdrawal Date
- 30-Sep-2004
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62D - IEC_SC_62D
- Parallel Committee
- IEC/SC 62D - IEC_SC_62D
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 15-Sep-2018
- Completion Date
- 15-Sep-2018
Relations
- Effective Date
- 28-Jan-2023
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Frequently Asked Questions
EN 60601-2-49:2001 is a standard published by CLC. Its full title is "Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment". This standard covers: Specifies requirements for the safety of multifunction patient monitoring equipment. Multifunction patient monitoring equipment is defined as a modular or pre-configured device including more than one physiological monitoring unit designed to collect information from a single patient and process it for monitoring purposes and to generate alarms.
Specifies requirements for the safety of multifunction patient monitoring equipment. Multifunction patient monitoring equipment is defined as a modular or pre-configured device including more than one physiological monitoring unit designed to collect information from a single patient and process it for monitoring purposes and to generate alarms.
EN 60601-2-49:2001 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-49:2001 has the following relationships with other standards: It is inter standard links to EN 60601-2-49:2015. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-49:2001 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/432. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
EN 60601-2-49:2001 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
SLOVENSKI STANDARD
01-junij-2002
0HGLFLQVNDHOHNWULþQDRSUHPD GHO 3RVHEQHYDUQRVWQH]DKWHYH]D
SDFLHQWRYRYHþIXQNFLMVNRQDG]RURYDOQRRSUHPR ,(&
Medical electrical equipment - Part 2-49: Particular requirements for the safety of
multifunction patient monitoring equipment (IEC 60601-2-49:2001)
Medizinische elektrische Geräte - Teil 2-49: Besondere Festlegungen für die Sicherheit
von multifunktionalen Patientenüberwachungsgeräten (IEC 60601-2-49:2001)
Appareils électromédicaux - Partie 2-49: Règles particulières de sécurité des appareils
de surveillance multifonction des patients (CEI 60601-2-49:2001)
Ta slovenski standard je istoveten z: EN 60601-2-49:2001
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
EUROPEAN STANDARD EN 60601-2-49
NORME EUROPÉENNE
EUROPÄISCHE NORM October 2001
ICS 11.040.55
English version
Medical electrical equipment
Part 2-49: Particular requirements for the safety
of multifunction patient monitoring equipment
(IEC 60601-2-49:2001)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-49: Règles particulières Teil 2-49: Besondere Festlegungen
de sécurité des appareils für die Sicherheit von multifunktionalen
de surveillance multifonction des patients Patientenüberwachungsgeräten
(CEI 60601-2-49:2001) (IEC 60601-2-49:2001)
This European Standard was approved by CENELEC on 2001-10-01. CENELEC 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 Central Secretariat or to any CENELEC 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 CENELEC member into its own language and
notified to the Central Secretariat has the same status as the official versions.
CENELEC members are the national electrotechnical committees of Austria, Belgium, Czech Republic,
Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands,
Norway, Portugal, Spain, Sweden, Switzerland and United Kingdom.
CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
Central Secretariat: rue de Stassart 35, B - 1050 Brussels
© 2001 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-2-49:2001 E
Foreword
The text of document 62D/409/FDIS, fu
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