EN 60601-2-37:2001/A1:2005
(Amendment)Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment
Superseded by EN 60601-2-37:2008
Medizinische elektrische Geräte - Teil 2-37: Besondere Festlegungen für die Sicherheit von Ultraschall-Geräten für die medizinische Diagnose und Überwachung
Appareils électromédicaux - Partie 2-37: Règles particulières de sécurité pour les appareils de diagnostic et de surveillance médicaux à ultrasons
Medicinska električna oprema – 2-37. del: Posebne varnostne zahteve za ultrazvočno medicinsko diagnostično in nadzorovalno opremo
General Information
- Status
- Withdrawn
- Publication Date
- 08-Feb-2005
- Withdrawal Date
- 31-Dec-2007
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62B - IEC_SC_62B
- Parallel Committee
- IEC/SC 62B - IEC_SC_62B
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 01-Oct-2010
- Completion Date
- 01-Oct-2010
Relations
- Effective Date
- 28-Jan-2023
- Effective Date
- 29-Jan-2023
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Frequently Asked Questions
EN 60601-2-37:2001/A1:2005 is a amendment published by CLC. Its full title is "Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment". This standard covers: Superseded by EN 60601-2-37:2008
Superseded by EN 60601-2-37:2008
EN 60601-2-37:2001/A1:2005 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment; 17.140.50 - Electroacoustics. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-37:2001/A1:2005 has the following relationships with other standards: It is inter standard links to EN 60601-2-37:2008, EN 60601-2-37:2001. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-37:2001/A1:2005 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 60601-2-37:2001/A1:2005 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 SIST EN 60601-2-
37:2002/A1:2005
STANDARD
junij 2005
Medicinska električna oprema – 2-37. del: Posebne varnostne zahteve za
ultrazvočno medicinsko diagnostično in nadzorovalno opremo
Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment
ICS 11.040.55; 17.140.50 Referenčna številka
© Standard je založil in izdal Slovenski inštitut za standardizacijo. Razmnoževanje ali kopiranje celote ali delov tega dokumenta ni dovoljeno
EUROPEAN STANDARD EN 60601-2-37/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM February 2005
ICS 11.040.55; 17.140.50
English version
Medical electrical equipment
Part 2-37: Particular requirements for the safety
of ultrasonic medical diagnostic and monitoring equipment
(IEC 60601-2-37:2001/A1:2004)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-37: Règles particulières Teil 2-37: Besondere Festlegungen
de sécurité pour les appareils für die Sicherheit von Ultraschall-Geräten
de diagnostic et de surveillance médicaux für die medizinische Diagnose
à ultrasons und Überwachung
(CEI 60601-2-37:2001/A1:2004) (IEC 60601-2-37:2001/A1:2004)
This amendment A1 modifies the European Standard EN 60601-2-37:2001; it was approved by
CENELEC on 2004-12-07. 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 Central Secretariat or to any CENELEC member.
This amendment exists in three official versions (English, French, German). A version in any other language
mad
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